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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
 ______________________________
FORM 10-Q
______________________________ 
ý
ýQUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the Quarterly Period Ended quarterly period ended December 31, 20172023
or
¨
¨TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
001-36587
(Commission File Number)
Image1.jpg
 _____________________________
Catalent, Inc.
(Exact name of registrant as specified in its charter)
_____________________________ 
     Delaware20-8737688
Delaware20-8737688
(State        (State or other jurisdiction of incorporation or organization)(I.R.S. Employer Identification No.)
14 Schoolhouse Road
                   Somerset, NJNew Jersey08873
(Address
                     (Address of principal executive offices)_______
(Zip code)
(732) 537-6200
Registrant's telephone number, including area code
__________________________________________________________________ 

Securities registered pursuant to Section 12(b) of the Act:
Title of each classTrading Symbol(s)Name of each exchange on which registered
Common Stock, $0.01 par value per shareCTLTNew York Stock Exchange

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.   Yes x¨  No¨
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).       x Yes ¨  No
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
Large accelerated filerx
Accelerated filer¨
¨
Non-accelerated filer¨
¨(Do not check if a smaller reporting company)
Smaller reporting company¨
¨
Emerging growth company¨
¨
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ¨
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).       ¨Yes    ¨ No x




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On February 2, 2018,January 31, 2024, there were 133,318,679180,737,675 shares of the Registrant's common stock, par value $0.01 per share, issued and outstanding.




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CATALENT, INC. and Subsidiaries

INDEX TO FORMIndex to Form 10-Q
For the Three and Six Months Ended December 31, 20172023
ItemPage
ItemPage
Part I.
Item 1.
Item 2.
Item 3.
Item 4.
Part II.
Item 1.
Item 1A.
Item 2.
Item 3.
Item 4.
Item 5.
Item 6.


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Special Note Regarding Forward-Looking Statements
In addition to historical information, this Quarterly Report on Form 10-Q may containof Catalent, Inc. (“Catalent” or the “Company”) contains “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, (the “Securities Act”), and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), which are subject to the “safe harbor” created by those sections. All statements, other than statements of historical facts, included in this Quarterly Report on Form 10-Q are forward-looking statements. In some cases, you can identify these forward-looking statements by the use of words such as “outlook,” “believes,” “expects,” “potential,” “continues,” “may,” “will,” “should,” “could,” “seeks,” “approximately,” “predicts,” “intends,” “plans,” “estimates,” “anticipates” or the negative version of these words or other comparable words.
These statements are based on assumptions and assessments made by our management in light of their experience and their perception of historical trends, current conditions, expected future developments, and other factors they believe to be appropriate. Any forward-looking statement is subject to various risks and uncertainties. Accordingly, there are or will be important factors that could cause actual outcomes or results to differ materially from those indicated in these statements.

Some of the factors that may cause actual results, developments and business decisions to differ materially from those contemplated by such forward-looking statements include, but are not limited to, those summarized below, in addition to those described more fully (i) from time to time in reports that we have filed or in the future may file with the Securities and Exchange Commission (the “SEC”), and (ii) under the section entitled “Risk Factors” in our Annual Report on Form 10-K for the fiscal year ended June 30, 20172023 (the "Fiscal 2023 10-K").

Risks Relating to Our Business and the following:Industry in Which We Operate


We participate in a highly competitive market,Actions of activist shareholders could impact the pursuit of our business strategies and increased competition may adversely affect our business.results of operations, financial condition, or share price.


We anticipate being subject to increasing focus by our investors, regulators, customers, and other stakeholders on environmental, social, and governance (“ESG”) matters.

Any failure to implement fully, monitor, and continuously improve our quality management strategy could lead to quality or safety issues and expose us to significant costs, potential liability, and adverse publicity.

We have experienced, and may continue to experience, productivity issues and higher-than-expected costs at certain of our facilities, which have resulted in, and may continue to result in, material and adverse impacts on our financial condition and results of operations.

The declining demand for various COVID-19 vaccines and treatments from both patients and governments around the world has affected and may continue to affect sales of the COVID-19 products we manufacture and our financial condition.

The demand for our offerings depends in part on our customers’ research and development and the clinical and market success of their products. Our business, financial condition and results of operations may be harmed if our customers spend less on, or are less successful in, these activities.


We are subject to product and other liability risks that could adversely affect our results of operations, financial condition, liquidity, and cash flows.

Failure to comply with existing and future regulatory requirements could adversely affect our results of operations and financial condition or result in claims from customers.

Failure to provide quality offerings to our customers could have an adverse effect on our business and subject us to regulatory actions or costly litigation.

The services and offerings we provide are highly exacting and complex, and if we encounter problems providing the services or support required, our business could suffer.

Our global operations are subject to economic, political, and regulatory risks, including the risks of changing regulatory standards or changing interpretations of existing standards, that could affect the profitability of our operations or require costly changes to our procedures.

The referendum in the United Kingdom (the "U.K.") and resulting decision of the U.K. government to consider exiting from the European Union could have future adverse effects on our revenues and costs, and therefore our profitability.

If we do not enhance our existing or introduce new technology or service offerings in a timely manner, our offerings may become obsolete over time, customers may not buy our offerings, and our revenue and profitability may decline.

We and our customers depend on patents, copyrights, trademarks, trade secrets, and other forms of intellectual property protections, but these protections may not be adequate.

Our future results of operations are subject to fluctuations in the costs, availability, and suitability of the components of the products we manufacture, including active pharmaceutical ingredients, excipients, purchased components, and raw materials.materials, and other supplies or equipment we need to run our business.


Changes in market access or healthcare reimbursement for our customers’ productsOur goodwill has been subject to impairment and may be subject to further impairment in the United States or internationally, including the possible repeal or replacement of the Affordable Care Act in the United States, could adversely affect our results of operations and financial condition by affecting demand for our offerings.


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As a global enterprise, fluctuations in the exchange rate of the U.S. dollar against foreign currenciesfuture, which could have a material adverse effect on our financial performance and results of operations.

The impact to our business of recently enacted U.S. tax legislation could differ materially from our current estimates.

Tax legislative or regulatory initiatives or challenges to our tax positions could adversely affect our results of operations, and financial condition.condition, or future operating results.


Our ability to use our net operating loss carryforwards and certain other tax attributes may be limited.


ChangesWe may acquire businesses and offerings that complement or expand our business or divest non-strategic businesses or assets. We may not be able to complete desired transactions, and such transactions, if executed, pose significant risks, including risks relating to our ability to successfully and efficiently integrate acquisitions or execute on dispositions and realize anticipated benefits therefrom. The failure to execute or realize the estimated futurefull benefits from any such transaction could have a negative effect on our operations and profitability.

We may become subject to litigation, other proceedings, and government investigations relating to us or our operations, and the ultimate outcome of any such matter may have an impact on our business, prospects, financial condition, and results of operations.
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Our global operations are subject to economic and political risks, including risks resulting from continuing inflation, disruptions to global supply chains, destabilization of a regional or national banking system, or from the Ukrainian-Russian war or the effect of the evolving nature of the recent war in Gaza between Israel and Hamas, which could affect the profitability of the business mayour operations or require that we establish an additional valuation allowance against all or some portion ofcostly changes to our net U.S. deferred tax assets.procedures.


We are dependent on key personnel.

We use advanced information and communication systems to run our operations, compile and analyze financial and operational data, and communicate among our employees, customers, and counter-parties, socounterparties, and the risks generally associated with information and communications systems could adversely affect our results of operations. We are continuously workingwork to install new, and upgrade existing, systems and provide employee awareness training around phishing, malware, and other cyber securitycybersecurity risks to enhance the protections available to us, but such protections may be inadequate to address malicious attacks or inadvertent compromises affecting data security or the operability of data security.such systems.


We engage, from time to time, in acquisitionsArtificial intelligence-based platforms present new risks and other transactions that may complement or expand our business or divest of non-strategic businesses or assets. We may not be able to complete such transactions, and such transactions, if executed, pose significant risks, including risks relatingchallenges to our abilitybusiness.
Our cash, cash equivalents, and financial investments could be adversely affected if the financial institutions in which we hold our cash, cash equivalents, and financial investments fail.

Risks Relating to successfully and efficiently integrate acquisitions and realize anticipated benefits therefrom. Our Indebtedness

The failure to execute or realize the full benefits from any such transaction could have a negative effect on our operations.

Our offerings or our customers’ products may infringe on the intellectual property rights of third parties.

We are subject to environmental, health, and safety laws and regulations, which could increase our costs and restrict our operations in the future.

We are subject to labor and employment laws and regulations, which could increase our costs and restrict our operations in the future.

Certainsize of our pension plans are underfunded,indebtedness and additional cash contributions we may make to increase the funding level will reduce the cash available for our business, such as the payment of our interest expense.

Our substantial leverageobligations associated with it could adversely affect our ability to raise additional capital to fund our operations, limit our ability to react to changes in the economy or in our industry or to deploy capital to grow our business, expose us to interest-rate risk to the extent of our variable ratevariable-rate debt, andor prevent us from meeting our obligations under our indebtedness. These risks may be increased in a recessionary environment, particularly as sources of capital may become less available or more expensive.


Despite our high indebtedness level, we and our subsidiaries are still capable of incurring significant additional debt, which could further exacerbate the risks associated with our substantial indebtedness.

Our interest expense on our variable-rate debt may continue to increase if and to the extent that policymakers combat inflation through interest-rate increases on benchmark financial products.

Despite the limitations in our debt agreements, we retain the ability to take certain actions that may interfere with our ability to timely pay our substantial indebtedness.

We may not be able to pay our indebtedness when it becomes due.

We are currently using and may in the future use derivative financial instruments to reduce our exposure to market risks from changes in interest rates on our variable-rate indebtedness or changes in currency exchange rates, and any such instrument may expose us to risks related to counterparty credit worthiness or non-performance of these instruments.

Risks Relating to Ownership of Our Common Stock

We do not presently maintain effective disclosure controls and procedures due to material weaknesses we have identified in our internal controls over financial reporting. Failure to remediate these material weaknesses or any other material weakness or significant deficiencies have resulted in a revision of our financial statements, in the future could result in material misstatements in our financial statements and have caused, and in the future could cause us to fail to timely meet our periodic reporting obligations.

Our stock price has historically been and may continue to be volatile, and a holder of shares of our Common Stock may not be able to resell such shares at or above the price such stockholder paid, or at all, and could lose all or part of such investment as a result.

Future sales, or the perception of future sales, of our Common Stock, by us or our existing stockholders could cause the market price for our Common Stock to decline.

We are no longer eligible to use the Form S-3 registration statement, which could impair our capital-raising activities.

Provisions in our organizational documents could delay or prevent a change of control.

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We caution you that the risks, uncertainties, and other factors referenced above may not contain all of the risks, uncertainties, and other factors that are important to you. In addition, we cannot assure you that we will realize the results, benefits, or developments that we expect or anticipate or, even if substantially realized, that they will result in the consequences or affect us or our business in the way expected. There can be no assurance that (i) we have correctly measured or identified all of the factors affecting our business or the extent of these factors’ likely impact, (ii) the available information with respect to these factors on which such analysis is based is complete or accurate, (iii) such analysis is correct, or (iv) our strategy, which is based in part on this analysis, will be successful. All forward-looking statements in this report apply only as of the date of this report or as of the date they were made and we undertake no obligation to publicly update or review any forward-looking statement, whether as a result of new information, future developments, or otherwise, except as required by law.
Social Media
We use our website (www.catalent.com)(catalent.com), our corporate Facebook page (https://www.facebook.com/(facebook.com/CatalentPharmaSolutions), LinkedIn page (linkedin.com/company/catalent-pharma-solutions/) and our corporate Twitter account (@catalentpharma) as channels for theof distribution of

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information. information concerning our activities, our offerings, our various businesses, and other related matters. The information we post through these channels may be deemed material. Accordingly, investors should monitor these channels, in addition to following our press releases, Securities and Exchange Commission ("SEC")SEC filings, and public conference calls and webcasts. The contents ofinformation contained on or accessible through our website, andour social media channels, areor any other website that we may maintain is not however, a part of this report.

Quarterly Report.
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PART I.    FINANCIAL INFORMATION


Item 1.
ITEM 1.     FINANCIAL STATEMENTS


Catalent, Inc. and Subsidiaries
Consolidated Statements of Operations
(Unaudited; Dollarsdollars in millions, except per share data)


Three Months Ended  
December 31,
Six Months Ended  
December 31,
2023202220232022
Net revenue$1,024 $1,149 $2,006 $2,171 
Cost of sales853 762 1,666 1,526 
Gross margin171 387 340 645 
Selling, general, and administrative expenses250 226 455 422 
Goodwill impairment (adjustments) charges(2)— 687 — 
Other operating expense, net35 23 36 25 
Operating (loss) earnings(112)138 (838)198 
Interest expense, net66 47 124 79 
Other expense (income), net(23)17 
(Loss) earnings before income taxes(182)114 (979)117 
Income tax expense (benefit)24 33 (14)36 
Net (loss) earnings$(206)$81 $(965)$81 
Earnings (loss) per share:
Basic
Net (loss) earnings$(1.13)$0.45 $(5.31)$0.45 
Diluted
Net (loss) earnings$(1.13)$0.44 $(5.31)$0.45 
 Three Months Ended  
 December 31,
 Six Months Ended  
 December 31,
 2017 2016 2017 2016
Net revenue$606.3
 $483.7
 $1,150.2
 $925.9
Cost of sales418.9
 335.8
 822.7
 653.9
Gross margin187.4
 147.9
 327.5
 272.0
Selling, general and administrative expenses114.3
 96.2
 221.3
 194.4
Impairment charges and (gain)/loss on sale of assets4.2
 0.5
 4.2
 0.5
Restructuring and other0.1
 3.3
 1.3
 4.4
Operating earnings68.8
 47.9
 100.7
 72.7
Interest expense, net27.2
 22.8
 51.5
 44.9
Other expense/(income), net13.6
 (1.8) 19.3
 (3.9)
Earnings from continuing operations, before income taxes28.0
 26.9
 29.9
 31.7
Income tax expense49.9
 9.5
 48.0
 9.7
Net earnings/(loss)$(21.9) $17.4
 $(18.1) $22.0
        
        
Earnings per share:       
Basic       
Net earnings/(loss)$(0.16) $0.14
 $(0.14) $0.18
Diluted  

   

Net earnings/(loss)$(0.16) $0.14
 $(0.14) $0.17












The accompanying notes are an integral part of these unaudited consolidated financial statements.

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Catalent, Inc. and Subsidiaries
Consolidated Statements of Comprehensive Income/(Loss)Loss
(Unaudited; Dollarsdollars in millions)



 Three Months Ended  
 December 31,
 Six Months Ended  
 December 31,
 2017 2016 2017 2016
Net earnings/(loss)$(21.9) $17.4
 $(18.1) $22.0
Other comprehensive income/(loss), net of tax       
Foreign currency translation adjustments(13.4) (64.4) 24.7
 (63.8)
Pension and other post-retirement adjustments0.5
 0.7
 0.9
 1.5
Available for sale investments(3.0) 15.3
 (6.4) 15.3
Other comprehensive income/(loss), net of tax(15.9) (48.4) 19.2
 (47.0)
Comprehensive income/(loss)$(37.8) $(31.0) $1.1
 $(25.0)
Three Months Ended  
December 31,
Six Months Ended  
December 31,
2023202220232022
Net (loss) earnings$(206)$81 $(965)$81 
Other comprehensive (loss) income, net of tax
Foreign currency translation adjustments37 118 (2)(17)
Pension and other post-retirement adjustments— — 
Net change in marketable securities— — 
Derivatives and hedges(7)— (2)14 
Other comprehensive income (loss), net of tax34 119 — (1)
Comprehensive (loss) income$(172)$200 $(965)$80 






















The accompanying notes are an integral part of these unaudited consolidated financial statements.

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Catalent, Inc. and Subsidiaries
Consolidated Balance Sheets
(Unaudited; Dollars in millions, except share and per share data)
December 31,
2023
June 30,
2023
ASSETS
Current assets:
Cash and cash equivalents$229 $280 
Trade receivables, net of allowance for credit losses of $42 and $46, respectively843 1,002 
Inventories775 777 
Prepaid expenses and other723 633 
Total current assets2,570 2,692 
Property, plant, and equipment, net of accumulated depreciation of $1,756 and $1,596, respectively3,777 3,682 
Other assets:
Goodwill2,351 3,039 
Other intangibles, net911 980 
Deferred income taxes55 55 
Other long-term assets324 329 
Total assets$9,988 $10,777 
LIABILITIES AND SHAREHOLDERS' EQUITY
Current liabilities:
Current portion of long-term obligations and other short-term borrowings$46 $536 
Accounts payable407 424 
Other accrued liabilities583 570 
Total current liabilities1,036 1,530 
Long-term obligations, less current portion4,959 4,313 
Pension liability101 100 
Deferred income taxes50 76 
Other liabilities155 147 
Commitment and contingencies (see Note 14)
Total liabilities6,301 6,166 
Shareholders' equity:
Common stock, $0.01 par value; 1.00 billion shares authorized at December 31, 2023 and June 30, 2023; 181 million and 180 million issued and outstanding at December 31, 2023 and June 30, 2023, respectively
Preferred stock, $0.01 par value; 100 million shares authorized at December 31, 2023 and June 30, 2023;0 shares issued and outstanding at December 31, 2023 and June 30, 2023— — 
Additional paid in capital4,742 4,701 
(Accumulated deficit) retained earnings(703)262 
Accumulated other comprehensive loss(354)(354)
Total shareholders' equity3,687 4,611 
Total liabilities and shareholders' equity$9,988 $10,777 

 December 31,
2017
 June 30,
2017
ASSETS   
Current assets:   
Cash and cash equivalents$329.5
 $288.3
Trade receivables, net427.9
 488.8
Inventories212.7
 184.9
Prepaid expenses and other105.4
 97.8
Total current assets1,075.5
 1,059.8
Property, plant, and equipment, net1,256.2
 995.9
Other assets:   
Goodwill1,408.3
 1,044.1
Other intangibles, net582.0
 273.1
Deferred income taxes34.3
 53.9
Other30.8
 27.5
Total assets$4,387.1
 $3,454.3
    
LIABILITIES AND SHAREHOLDERS' EQUITY
Current liabilities:   
Current portion of long-term obligations and other short-term borrowings$69.9
 $24.6
Accounts payable164.3
 163.2
Other accrued liabilities249.8
 281.2
Total current liabilities484.0
 469.0
Long-term obligations, less current portion2,672.5
 2,055.1
Pension liability127.3
 129.5
Deferred income taxes40.7
 31.7
Other liabilities57.1
 45.5
Commitment and contingencies (see Note 13)   
    
Shareholders' equity/(deficit):   
Common stock $0.01 par value; 1.0 billion shares authorized on December 31, 2017 and June 30, 2017, 133,318,039 and 125,049,867 issued and outstanding on December 31, 2017 and June 30, 2017, respectively.1.3
 1.3
Preferred stock $0.01 par value; 100 million authorized on December 31, 2017 and June 30, 2017, 0 issued and outstanding on December 31, 2017 and June 30, 2017.
 
Additional paid in capital2,272.9
 1,992.0
Accumulated deficit(973.8) (955.7)
Accumulated other comprehensive income/(loss)(294.9) (314.1)
Total shareholders' equity1,005.5
 723.5
Total liabilities and shareholders' equity$4,387.1
 $3,454.3

The accompanying notes are an integral part of these unaudited consolidated financial statements.

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Catalent, Inc. and Subsidiaries
Consolidated Statement of Changes in Shareholders' Equity/(Deficit)Equity
(Unaudited; Dollarsdollars in millions, except share data in thousands)
 

 Shares of Common Stock 
Common
Stock
 Additional
Paid in
Capital
 
Accumulated
Deficit
 
Accumulated
Other
Comprehensive
Income/(Loss)
 
Total
Shareholders'
Equity/ (Deficit)
Balance at June 30, 2017125,049.9
 $1.3
 $1,992.0
 $(955.7) $(314.1) $723.5
Equity offering, sale of common stock7,354.2
 
 277.8
     277.8
Share issuances related to equity-based
     compensation
913.9
 
       
Equity compensation    15.5
     15.5
Cash paid, in lieu of equity, for tax
     withholding
    (12.4)     (12.4)
Net earnings/(loss)      (18.1)   (18.1)
Other comprehensive income/(loss), net
     tax
        19.2
 19.2
Balance at December 31, 2017133,318.0
 $1.3
 $2,272.9
 $(973.8) $(294.9) $1,005.5

Three Months Ended December 31, 2023
Shares of Common StockCommon StockAdditional Paid in CapitalAccumulated DeficitAccumulated Other Comprehensive LossTotal Shareholders' Equity
Balance at September 30, 2023180,521 $2 $4,724 $(497)$(388)$3,841 
Share issuances related to stock-
     based compensation
147 — — — — — 
Stock-based compensation— — 16 — — 16 
Employee stock purchase plan— — — — 
Net loss— — — (206)— (206)
Other comprehensive income, net
of tax
— — — — 34 34 
Balance at December 31, 2023180,668 $2 $4,742 $(703)$(354)$3,687 





Three Months Ended December 31, 2022
Shares of Common StockCommon StockAdditional Paid in CapitalRetained EarningsAccumulated Other Comprehensive LossTotal Shareholders' Equity
Balance at September 30, 2022179,901 $2 $4,674 $538 $(514)$4,700 
Share issuances related to stock-
     based compensation
87 — — — — — 
Stock-based compensation— — 10 — — 10 
Cash paid, in lieu of
   equity, for tax withholding
   obligations
— — (2)— — (2)
Employee stock purchase plan— — — — 
Net earnings— — — 81 — 81 
Other comprehensive loss, net
       of tax
— — — — 119 119 
Balance at December 31, 2022179,988 $2 $4,686 $619 $(395)$4,912 






The accompanying notes are an integral part of these unaudited consolidated financial statements.

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Catalent, Inc. and Subsidiaries
Consolidated StatementsStatement of Cash FlowsChanges in Shareholders' Equity
(Unaudited; Dollarsdollars in millions)millions, except share data in thousands)

 Six Months Ended 
 December 31,
 2017 2016
CASH FLOWS FROM OPERATING ACTIVITIES:   
Net earnings/(loss)$(18.1) $22.0
Adjustments to reconcile earnings from continued operations to net cash from operations:   
Depreciation and amortization85.8
 71.3
Non-cash foreign currency transaction (gain)/loss, net7.1
 (3.4)
Amortization and write off of debt financing costs2.5
 4.3
Asset impairments and (gain)/loss on sale of assets4.2
 0.5
Reclassification of financing fees paid11.8
 
Equity compensation15.5
 11.8
Provision/(benefit) for deferred income taxes35.6
 0.9
Provision for bad debts and inventory3.5
 3.3
Change in operating assets and liabilities:   
Decrease/(increase) in trade receivables104.6
 41.4
Decrease/(increase) in inventories
 (17.9)
Increase/(decrease) in accounts payable(0.4) (14.6)
Other assets/accrued liabilities, net - current and non-current(76.1) (23.6)
Net cash provided by operating activities176.0
 96.0
CASH FLOWS FROM INVESTING ACTIVITIES:   
Acquisition of property and equipment and other productive assets(82.9) (54.1)
Proceeds from sale of property and equipment1.8
 1.3
Proceeds from sale of subsidiaries3.4
 
Payment for acquisitions, net of cash acquired(748.0) (85.7)
Net cash (used in) investing activities(825.7) (138.5)
CASH FLOWS FROM FINANCING ACTIVITIES:   
Net change in other borrowings(0.6) (5.6)
Proceeds from borrowing, net442.6
 397.4
Payments related to long-term obligations(9.4) (209.2)
Financing fees paid(15.6) (6.4)
Proceeds from sale of common stock, net277.8
 
Cash paid, in lieu of equity, for tax withholding obligations(12.4) (0.5)
Net cash provided by financing activities682.4
 175.7
Effect of foreign currency on cash8.5
 (9.0)
NET INCREASE/(DECREASE) IN CASH AND EQUIVALENTS41.2
 124.2
CASH AND EQUIVALENTS AT BEGINNING OF PERIOD288.3
 131.6
CASH AND EQUIVALENTS AT END OF PERIOD$329.5
 $255.8
SUPPLEMENTARY CASH FLOW INFORMATION:   
Interest paid$41.5
 $39.4
Income taxes paid, net$8.0
 $19.7


Six months ended December 31, 2023
Shares of Common StockCommon StockAdditional Paid in CapitalRetained EarningsAccumulated Other Comprehensive LossTotal Shareholders' Equity
Balance at June 30, 2023180,273 $2 $4,701 $262 $(354)$4,611 
Share issuances related to stock-
     based compensation
395 — — — — — 
Stock-based compensation— — 35 — — 35 
Exercise of stock options— — — — 
Employee stock purchase plan— — — — 
Net loss— — — (965)— (965)
Other comprehensive income,
net of tax
— — — — — — 
Balance at December 31, 2023180,668 $2 $4,742 $(703)$(354)$3,687 





Six Months Ended December 31, 2022
Shares of Common StockCommon StockAdditional Paid in CapitalAccumulated DeficitAccumulated Other Comprehensive LossTotal Shareholders' Equity
Balance at June 30, 2022179,302 $2 $4,649 $518 $(394)$4,775 
Share issuances related to stock-
     based compensation
686 — — — — — 
Stock-based compensation— — 29 — — 29 
Exercise of stock options— — — — 
Employee stock purchase plan— — — — 
Net earnings— — — 81 — 81 
Other comprehensive income,
net of tax
— — — — (1)(1)
Balance at December 31, 2022179,988 $2 $4,686 $599 $(395)$4,892 






The accompanying notes are an integral part of these unaudited consolidated financial statements.

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Catalent, Inc. and Subsidiaries
Consolidated Statements of Cash Flows
(Unaudited; dollars in millions)

Six Months Ended December 31,
20232022
CASH FLOWS FROM OPERATING ACTIVITIES:
Net (loss) earnings$(965)$81 
Adjustments to reconcile net (loss) earnings to net cash from operations:
Depreciation and amortization233 202 
Goodwill impairment charges687 — 
Non-cash foreign currency transaction loss, net11 
Non-cash restructuring charges
Amortization of debt issuance costs
Impairments charges and loss/gain on sale of assets, net14 (1)
Stock-based compensation35 29 
Provision for deferred income taxes(27)13 
Provision for bad debts and inventory44 67 
Pension settlement charges— 
Change in operating assets and liabilities:
Decrease in trade receivables165 148 
Increase in inventories(46)(180)
Decrease in accounts payable(40)(68)
Other assets/accrued liabilities, net—current and non-current(85)(181)
Net cash provided by operating activities42 122 
CASH FLOWS USED IN INVESTING ACTIVITIES:
Acquisition of property, equipment, and other productive assets(178)(317)
Proceeds from maturity of marketable securities— 61 
Proceeds from sale of property and equipment
Payment for acquisitions, net of cash acquired— (474)
Payment for investments(2)(1)
Net cash used in investing activities(179)(724)
CASH FLOWS FROM FINANCING ACTIVITIES:
Proceeds from borrowings815 625 
Payments related to long-term obligations(722)(32)
Financing fees paid(16)(4)
Exercise of stock options
Other financing activities
Net cash provided by financing activities84 597 
Effect of foreign currency exchange on cash and cash equivalents(2)
NET DECREASE IN CASH AND CASH EQUIVALENTS(51)(7)
CASH AND CASH EQUIVALENTS AT BEGINNING OF PERIOD280 449 
CASH AND CASH EQUIVALENTS AT END OF PERIOD$229 $442 
SUPPLEMENTARY CASH FLOW INFORMATION:
Interest paid$112 $83 
Income taxes paid, net$31 $38 
Non-cash purchase of property, equipment, and other productive assets$21 $13 




The accompanying notes are an integral part of these unaudited consolidated financial statements.
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Catalent, Inc.
Notes to Unaudited Consolidated Financial Statements

1.    BASIS OF PRESENTATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
1.BASIS OF PRESENTATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Business
Catalent, Inc. (“Catalent”(Catalent or the “Company”Company) directly and wholly owns PTS Intermediate Holdings LLC (“(Intermediate Holdings”Holdings). Intermediate Holdings directly and wholly owns Catalent Pharma Solutions, Inc. (“(Operating Company”Company). The financial results of Catalent are comprised of the financial results of Operating Company and its subsidiaries on a consolidated basis.
Basis of Presentation
The accompanying unaudited consolidated financial statements have been prepared in accordance with generally accepted accounting principles in the United States (“GAAP”(“U.S. GAAP) for interim financial information and with the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, they do not include all of the information and notes required by U.S. GAAP for complete financial statements. In the opinion of management, all adjustments (consisting of normal recurring adjustments) considered necessary for a fair presentation have been included. Operating results for the three and six months ended December 31, 20172023 are not necessarily indicative of the results that may be expected for the year ending June 30, 2018.2024. The consolidated balance sheet at June 30, 20172023 has been derived from the audited consolidated financial statements at that date but does not include all of the information and footnotes required by U.S. GAAP for complete financial statements. For further information on the Company's accounting policies and footnotes, refer to the consolidated financial statements and footnotesnotes thereto included in the Company’s Annual Report on Form 10-K for the year ended June 30, 20172023 filed with the Securities and Exchange Commission ("SEC"(the “SEC”). on December 8, 2023.
UseReportable Segments
Set forth below is a summary description of Estimatesthe Company's two current operating and reportable segments.

Biologics—The preparation of financial statements in conformity with GAAP requires management to make estimatesBiologics segment provides development and assumptions that affect amounts reported in the financial statements and accompanying notes. Such estimates include, but are not limited to, allowancemanufacturing for doubtful accounts, inventory and long-lived asset valuation, goodwillbiologic proteins; cell, gene, and other intangible asset valuationnucleic acid therapies; plasmid DNA ("pDNA"); induced pluripotent stem cells ("iPSCs"), and impairment, equity-based compensation, income taxes,oncolytic viruses; and pension plan assetvaccines. It also provides formulation, development, and liability valuation. Actual amounts may differ from these estimated amounts.manufacturing for parenteral dose forms, including vials, prefilled syringes, and cartridges; analytical development and testing services for large molecules.

Pharma and Consumer Health—The Pharma and Consumer Health segment comprises the Company’s market-leading capabilities for complex oral solids, softgel formulations, Zydis® fast-dissolve technologies, and gummy, soft chew, and lozenge dosage forms; formulation, development, and manufacturing platforms for oral, nasal, inhaled, and topical dose forms; and clinical trial development and supply services.

Each segment reports through a separate management team and ultimately reports to the Company's President and Chief Executive Officer, who is designated as the Chief Operating Decision Maker for segment reporting purposes. The Company's operating segments are the same as its reportable segments.

Foreign Currency Translation
The financial statements of the Company’s operations outside the U.S. are generally measured using the local currency as the functional currency. Adjustments to translate the assets and liabilities of these foreign operations outside the United States (“U.S.”) into U.S. dollars are accumulated as a component of other comprehensive income/(loss)income utilizing period-end exchange rates. Since July 1, 2018, the Company has accounted for its Argentine operations as highly inflationary.
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Concentrations of Credit Risk and Major Customers
Concentration of credit risk, with respect to accounts receivable, is limited due to the large number of customers and their dispersion across different geographic areas. The currency fluctuations related to certain long-term inter-company loans deemed to not be repayablecustomers are primarily concentrated in the foreseeable futurepharmaceutical, biopharmaceutical and consumer products industries. The Company does not normally require collateral or any other security to support credit sales. The Company performs ongoing credit evaluations of its customers’ financial conditions and maintains reserves for credit losses. Such losses historically have been recorded within cumulative translation adjustment, a componentthe Company’s expectations.
As of other comprehensive income/(loss). In addition,December 31, 2023 and June 30, 2023, the currency fluctuationCompany had one customer that represented 27% and 20%, respectively, of its aggregate net trade receivables and current contract asset values, primarily associated with the portionCompany's Biologics segment. After performing a risk assessment of the Company’s euro-denominated debt designated as a net investment hedge is included as a component of other comprehensive income/(loss). Foreign currency transaction gains and losses calculated by utilizing weighted average exchange rates for the period are included in the consolidated statements of operations in the other (income)/expense, net line item. Foreign currency translation gains and losses generated from inter-company loans that are long-term in nature, but may be repayable in the foreseeable future, are also recorded within the other (income)/expense, net line item on the consolidated statements of operations.
Revenue Recognition
In accordance with Accounting Standards Codification ("ASC") 605 Revenue Recognition, the Company recognizes revenue when persuasive evidence of an arrangement exists, product delivery has occurred or the services have been rendered, the price is fixed or determinable and collectability is reasonably assured. In cases wherethis customer, the Company has multiple contracts with the same customer,determined that a reserve is not warranted as of December 31, 2023. Additionally, the Company evaluates those contracts to assess ifhad one customer in its Biologics segment that represented approximately 16% of consolidated net revenue during the contracts are linked or are separate arrangements. Factors the Company considers include the timing of negotiation, interdependency with other contracts or elements and payment terms. The Company and its customers generally view each contract discussion as a separate arrangement.
Manufacturing and packaging service revenue is recognized upon delivery of the product in accordance with the terms of the contract, which specify when transfer of title and risk of loss occurs. Some of the Company’s manufacturing contracts with

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its customers have annual minimum purchase requirements. At the end of the contract year, revenue is recognized for the unfilled purchase obligation in accordance with the contract terms. Development service contracts generally take the form of a fee-for-service arrangement. After the Company has evidence of an arrangement, the price is determinable and there is a reasonable expectation regarding payment, the Company recognizes revenue at the point in time the service obligation is completed and accepted by the customer. Examples of output measures include a formulation report, analytical and stability testing, clinical batch production or packaging and the storage and distribution of a customer’s clinical trial material. Development service revenue is primarily driven by the Company’s Drug Delivery Solutions segment.
Arrangements containing multiple elements, including service arrangements, are accounted for in accordance with the provisions of ASC 605-25Revenue Recognition—Multiple-Element Arrangements. The Company determines the separate units of account in accordance with ASC 605-25. If the deliverable meets the criteria of a separate unit of accounting, the arrangement consideration is allocated to each element based upon its relative selling price. In determining the best evidence of selling price of a unit of account, the Company utilizes vendor-specific objective evidence (“VSOE”), which is the price the Company charges when the deliverable is sold separately. When VSOE is not available, management uses relevant third-party evidence (“TPE”) of selling price, if available. When neither VSOE nor TPE of selling price exists, management uses its best estimate of selling price.
Goodwill
The Company accounts for purchased goodwill and intangible assets with indefinite lives in accordance with ASC 350 Goodwill, Intangible and Other Assets. Under ASC 350, goodwill and intangible assets with indefinite lives are not amortized, but instead are tested for impairment at least annually. The Company's annual goodwill impairment test was conducted as of April 1, 2017. The Company assesses goodwill for possible impairment by comparing the carrying value of its reporting units to their fair values. The Company determines the fair value of its reporting units utilizing estimated future discounted cash flows and incorporates assumptions that it believes marketplace participants would utilize. In addition, the Company uses comparative market information and other factors to corroborate the discounted cash flow results.
Property and Equipment and Other Definite Lived Intangible Assets
Property and equipment are stated at cost. Depreciation expense is computed using the straight-line method over the estimated useful lives of the assets, including capital lease assets that are amortized over the shorter of their useful lives or the terms of the respective leases. The Company generally uses the following ranges of useful lives for its property and equipment categories: buildings and improvements — 5 to 50 years; machinery and equipment — 3 to 10 years; and furniture and fixtures — 3 to 7 years. Depreciation expense was $30.7 million and $58.3 million for the three and six months ended December 31, 2017, respectively,2023. The Company had one customer that represented approximately 13% of net revenue and $24.4 million and $49.2 million foranother customer that represented approximately 10% of net revenue during the three andmonths ended December 31, 2022. For the six months ended December 31, 2016,2022, the Company had one customer that represented 11% of net revenue and two customers that each represented 10% of net revenue.
Depreciation
Depreciation expense was $88 million and $69 million for the three months ended December 31, 2023 and 2022, respectively. Depreciation expense was $166 million and $135 million for the six months ended December 31, 2023 and 2022, respectively. Depreciation expense includes amortization of assets related to capitalfinance leases. The Company charges repairs and maintenance costs to expense as incurred.
Amortization
Amortization expense related to other intangible assets was $33 million and $34 million for the three months ended December 31, 2023 and 2022, respectively. Amortization expense related to other intangible assets was $67 million for both the six months ended December 31, 2023 and 2022.
Research and Development Costs
The Company expenses research and development costs as incurred. Research and development costs amounted to $4 million for both the three months ended December 31, 2023 and 2022. Research and development costs amounted to $8 million and $9 million for the six months ended December 31, 2023 and 2022, respectively.
2.    REVENUE RECOGNITION

The Company recognizes revenue in accordance with ASC 606, Revenue from Contracts with Customers. The Company generally earns its revenue by supplying goods or providing services under contracts with its customers in three primary revenue streams: manufacturing and commercial product supply, development services, and clinical supply services. The Company measures the revenue from customers based on the consideration specified in its contracts, excluding any sales incentive or amount collected on behalf of a third party, that the Company expects to be entitled to receive in exchange for transferring the promised goods to and/or performing services for the customer (the “Transaction Price”). To the extent the Transaction Price includes variable consideration, the Company estimates the amount of capitalized interest was immaterialvariable consideration that should be included in the Transaction Price utilizing either the expected value method or the most likely amount method, depending on which method is expected to better predict the amount of consideration to which the Company will be entitled. The value of variable consideration is included in the Transaction Price if, and to the extent, it is probable that a significant reversal of the amount of cumulative revenue recognized will not occur when the uncertainty associated with the variable consideration is subsequently resolved. These estimates are re-assessed each reporting period, as required, and any adjustment required is recorded on a cumulative catch-up basis, which would affect revenue and net income in the period of adjustment.

The Company’s customer contracts generally include provisions entitling the Company to a termination penalty when the customer terminates prior to the contract’s nominal end date. The termination penalties in customer contracts vary but are generally considered substantive for all periods presented.
Intangible assets with finite lives, primarily including customer relationships, patentsaccounting purposes and trademarks are amortized over their useful lives.create enforceable rights and obligations throughout the stated durations of the contracts. The Company evaluatesaccounts for a contract termination as a contract modification in the recoverabilityperiod in which the customer gives notice of its other long-lived assets, including amortizing intangible assets, if circumstances indicate impairment may have occurred pursuant to ASC 360 Property, Plant and Equipment. This analysis is performed by comparing the respective carrying valuestermination. The determination of the assetscontract termination penalty is based on the terms stated in the relevant customer agreement. As of the modification date, the Company updates its estimate of the Transaction Price using the expected value method, subject to constraints, and to the currentextent that it is probable that a significant reversal in the amount of cumulative revenue recognized will not occur when the uncertainty associated with the variable consideration is subsequently resolved. These estimates are re-assessed each reporting period, as required, and expected future cash flows,any adjustment required is recorded on a cumulative catch-up basis, which would affect revenue and net income in the period of adjustment.
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Where multiple performance obligations exist in a single contract, the Company allocates consideration to each performance obligation using the “relative standalone selling price” as defined under ASC 606. Generally, the Company utilizes observable standalone selling prices in its allocations of consideration. If observable standalone selling prices are not available, the Company estimates the applicable standalone selling price using a cost-plus-margin approach or an un-discounted basis, to be generated from such assets. If such analysis indicatesadjusted market assessment approach, in each case, representing the amount that the carrying value of these assets is not recoverable, the carrying value of such assets is reduced to fair value through a charge to the consolidated statements of operations. Fair value is determined based on assumptions the Company believes marketplace participants would utilizethe market is willing to pay for the applicable service. Payment is typically due 30 to 45 days following the invoice date, based on the payment terms set forth in the applicable customer agreement.

The Company generally expenses sales commissions as incurred because either the amortization period is one year or less, or the balance with an amortization period greater than one year is not material.

Customer contracts that include commitments by the Company to make facility space or equipment available may be deemed to include lease components, which are evaluated under ASC 842, Leases. For arrangements that contain both lease and comparable marketplace informationnon-lease components, consideration in similar arm's length transactions. Impairment chargesthe contract is allocated on a relative standalone selling-price basis. Determining the lease term and contract term of non-lease components, as well as the variable and fixed consideration in these arrangements, including when variability is resolved, often requires management judgment in order to determine the allocation to the lease and non-lease components.
Manufacturing & Commercial Product Supply Revenue

Manufacturing and commercial product supply revenue consists of revenue earned by manufacturing products supplied to customers under long-term commercial supply arrangements. In these arrangements, the customer typically owns and supplies the active pharmaceutical ingredient (“API”) or other proprietary materials used in the manufacturing process. The contract generally includes the terms of the manufacturing services and related product quality assurance procedures to comply with regulatory requirements. Due to the regulated nature of the Company’s business, these contract terms are highly interdependent and, therefore, are considered to be a single combined performance obligation. The transaction price is generally stated in the agreement as a fixed price per unit, with no contractual provision for a refund or price concession. In most circumstances, control is transferred to the customer over time, creating a corresponding right to recognize the related revenue, because there is no alternative use to the Company for the asset created and the Company has an enforceable right to payment for performance completed as of that date. The selection of the method for measuring progress towards the completion of the Company’s performance obligation requires judgment and is based on the nature of the products to be manufactured. For the majority of the Company’s arrangements, progress is measured based on the units of product that have successfully completed the contractually required product quality assurance process, because the conclusion of that process defines the time when the applicable contract and the related regulatory requirements permit the customer to exercise control over the product’s disposition. The customer is typically responsible for arranging the shipping and handling of product following completion of the quality assurance process. Payment is typically due 30 to 45 days after invoice date, based on the payment terms set forth in the applicable customer agreement.

Beginning in the third quarter of fiscal 2023, the Company began recognizing commercial revenue for certain contracts in its Biologics segment that have a notably long manufacturing cycle, and for which the customer exercises control over the product throughout the manufacturing process. For these contracts, revenue is recognized over time and progress is measured using an input method based on effort expended, which provides an appropriate depiction of the Company’s progress toward fulfilling its performance obligation.

Development Services and Clinical Supply Revenue

Development services contracts generally take the form of short-term, fee-for-service arrangements. Performance obligations vary, but frequently include biologic cell-line development, performing formulation, analytical stability, or other services related to definite lived intangible assetsproduct development, and property, plantproviding manufacturing services for products that are under development or otherwise not intended for commercial sale. They can also include a combination of the following services: the manufacturing, packaging, storage, distribution, destruction, and equipment wereinventory management of customer clinical trial material, as well as the sourcing of comparator drug products on behalf of customers to be used in clinical trials to compare performance with the drug under clinical investigation. The transaction prices for these arrangements are fixed and include amounts stated in the contracts for each promised service, and each service is generally considered to be a separate performance obligation. In most instances, the Company recognizes revenue over time because there is no alternative use to the Company for the asset created and the Company has an enforceable right to payment for performance completed as of that date.

The Company measures progress toward the completion of its performance obligations satisfied over time based on the nature of the services to be performed. For certain types of arrangements, revenue is recognized over time and measured using
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an output method based on the completion of tasks and activities that are performed to satisfy a performance obligation. For certain types of arrangements, revenue is recognized over time and measured using an input method based on effort expended. Each of these methods provides an appropriate depiction of the Company’s progress toward fulfilling its performance obligations for its respective arrangement. In certain development services arrangements that require a portion of the contract consideration to be received in advance at the commencement of the contract, such advance payment is initially recorded as a contract liability. In certain clinical supply arrangements, revenue is recognized at the point in time when control transfers, which occurs upon either the delivery of the related output of the service to the customer or the completion of quality testing with respect to the product, and the Company has an enforceable right to payment based on the terms of the arrangement.

The Company records revenue for comparator sourcing arrangements on a net basis because it is acting as an agent that does not materialcontrol the product or service before it is transferred to the customer. Payment for comparator sourcing activity is typically received in advance at the commencement of the contract and is initially recorded as a contract liability.

The Company generally expenses sales commissions as incurred because either the amortization period is one year or less, or the balance with an amortization period greater than one year is not material.
The following tables reflect net revenue for the three and six months ended December 31, 20172023 and 2016.2022, by type of activity and reportable segment (in millions):
Research and Development Costs
Three Months Ended December 31, 2023BiologicsPharma and Consumer HealthTotal
Manufacturing & commercial product supply$278 $373 $651 
Development services & clinical supply160 214 374 
Total$438 $587 $1,025 
Inter-segment revenue elimination(1)
Combined net revenue$1,024 
The Company expenses research and development costs as incurred. Costs incurred in connection with the development of new offerings and manufacturing process improvements are recorded within selling, general and administrative expenses. Such research and development costs included in selling, general and administrative expenses amounted to $1.5 million and $3.3 million for the three and six months ended December 31, 2017, respectively, and $1.5 million and $3.0 million for the three and six months ended December 31, 2016, respectively. Costs incurred in connection with research and development services the Company provides to customers and services performed in support of the commercial manufacturing process for customers are recorded within cost of sales. Such research and development costs included in cost of sales amounted to $12.4 million and $22.4 million for the three and six months ended December 31, 2017, respectively, and $11.0 million and $21.3 million for the three and six months ended December 31, 2016, respectively.

Three Months Ended December 31, 2022BiologicsPharma and Consumer HealthTotal
Manufacturing & commercial product supply$76 $364 $440 
Development services & clinical supply504 206 710 
Total$580 $570 $1,150 
Inter-segment revenue elimination(1)
Combined net revenue$1,149 

Six Months Ended December 31, 2023BiologicsPharma and Consumer HealthTotal
Manufacturing & commercial product supply$560 $707 $1,267 
Development services & clinical supply326 414 740 
Total$886 $1,121 $2,007 
Inter-segment revenue elimination(1)
Combined net revenue$2,006 

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Six Months Ended December 31, 2022BiologicsPharma and Consumer HealthTotal
Manufacturing & commercial product supply$171 $678 $849 
Development services & clinical supply932 391 1,323 
Total$1,103 $1,069 $2,172 
Inter-segment revenue elimination(1)
Combined net revenue$2,171 
Earnings / (Loss) Per Share


The Company reports net earnings/(loss) per share in accordance with ASC 260Earnings per Share. Under ASC 260, basic earnings per share, which excludes dilution, is computed by dividing net earnings or loss available to common stockholdersfollowing table allocates revenue by the weighted average number of common shares outstanding forlocation where the period. Diluted earnings per share reflectsgoods were made or the potential dilution caused by securities that could be exercised or converted into common shares, and is computed by dividing net earnings or loss available to common stockholders by the weighted average of common shares outstanding plus the dilutive potential common shares. Diluted earnings per share includes in-the-money stock options, restricted stock units, and unvested restricted stock using the treasury stock method. During a loss period, the assumed exercise of in-the-money stock options has an anti-dilutive effect, and, therefore, these instruments are excluded from the computation of diluted earnings per share.service performed:
Equity-Based Compensation
The Company accounts for its equity-based compensation awards pursuant to ASC 718 Compensation—Stock Compensation. ASC 718 requires companies to recognize compensation expense using a fair value based method for costs related to share-based payments including stock options and restricted stock units. The expense is measured based on the grant date fair value of the awards, and the expense is recorded over the applicable requisite service period using the accelerated attribution method. Forfeitures are recognized as and when they occur. In the absence of an observable market price for a share-based award, the fair value is based upon a valuation methodology that takes into consideration various factors, including the exercise price of the award, the expected term of the award, the current price of the underlying shares, the expected volatility of the underlying share price based on peer companies, the expected dividends on the underlying shares and the risk-free interest rate.
The terms of the Company’s equity-based compensation plans permit an employee holding vested stock options to elect to have the Company withhold a portion of the shares otherwise issuable upon the employee's exercise of the option, a so-called "net settlement transaction," as a means of paying the exercise price meeting tax withholding requirements, or both.
Marketable Securities

Marketable securities consist of investments that have a readily determinable fair value based on quoted market price of the investment, which is considered a Level 1 fair value measurement. Under ASC 320, Investments—Debt and Equity Securities, these investments are classified as available-for-sale and are reported at fair value in other current assets on the Company's consolidated balance sheet. Unrealized holding gains and losses are reported within accumulated other comprehensive income/(loss). Under the Company's accounting policy, a decline in the fair value of marketable securities is deemed to be "other than temporary" and such marketable securities are generally considered to be impaired if their fair value is less than the Company's cost basis for a period based on the particular facts and circumstances surrounding the investment. If a decline in the fair value of a marketable security below the Company's cost basis is determined to be other than temporary, such marketable security is written down to its estimated fair value as a new cost basis and the amount of the write-down is included in earnings as an impairment charge.


Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)2023202220232022
United States$653 $734 $1,298 $1,432 
Europe324 356 599 630 
Other86 88 173 169 
Elimination of revenue attributable to multiple locations(39)(29)(64)(60)
Total$1,024 $1,149 $2,006 $2,171 
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Contract Liabilities
Recent Financial Accounting Standards
Recently Adopted Accounting Standards
In July 2015,Contract liabilities relate to cash consideration that the Financial Accounting Standards Board (the "FASB") issued Accounting Standards Update ("ASU") 2015-11, SimplifyingCompany receives in advance of satisfying the Measurement of Inventory, which requires an entity to measure inventory at lower of costrelated performance obligations. The contract liabilities balances (current and net realizable value. Net realizable value is the estimated selling prices in the ordinary course of business, less reasonably predictable costs of completion, disposal and transportation. The ASU is effective for public reporting entities in fiscal years beginning after December 15, 2016. The Company adopted this ASU prospectively in fiscal 2018. The adoption of this ASU did not have any material impact to the Company's consolidated financial statements.
In August 2016, the FASB issued ASU 2016-15 Statement of Cash Flows (Topic 230): Classification of Certain Cash Receipts and Cash Payments, which provides clarification on the presentation and classification of certain cash receipts and cash payments in the statement of cash flows. The guidance will be effective for publicly reporting entities in fiscal years beginning after December 15, 2017, and interim periods within those fiscal years. Early adoption is permitted in any interim or annual period. The Company early adopted this ASU retrospectively in fiscal 2018. The adoption of this ASU did not have any material impact to the Company's consolidated financial statements.
New Accounting Standards Not Adoptednon-current) as of December 31, 20172023 and June 30, 2023 are as follows:
In August 2017, the FASB issued ASU 2017-12, Derivatives and Hedging (Topic 815): Targeted Improvements to Accounting for Hedging Activities, which reduces the complexity of and simplifies the application of hedge accounting by preparers. The ASU
(Dollars in millions)
Balance at June 30, 2023$180 
Balance at December 31, 2023$219 
Revenue recognized in the period from amounts included in contracts liability at the beginning of the period:$(114)

Contract liabilities that will be effectiverecognized within 12 months of December 31, 2023 are accounted for fiscal years beginningin Other accrued liabilities and those that will be recognized longer than 12 months after December 15, 2018,31, 2023 are accounted for in Other liabilities.

Contract Assets
Contract assets primarily relate to the Company's conditional right to receive consideration for services that have been performed for customers as of December 31, 2023 relating to the Company's development and interim periodscommercial services but had not yet been invoiced as of December 31, 2023. Contract assets are transferred to trade receivables, net when the Company’s right to receive the consideration becomes unconditional. Contract assets totaled $495 million and $417 million as of December 31, 2023 and June 30, 2023, respectively. Contract assets expected to transfer to trade receivables within those years. Early adoption12 months are accounted for within Prepaid expenses and other. Contract assets expected to transfer to trade receivables longer than 12 months are accounted for within Other long-term assets.
As of December 31, 2023, the Company's aggregate contract asset balance increased $78 million or 19% compared to June 30, 2023. The majority of this increase is permitted. The Company is currently evaluating the impact of adopting this guidance on its consolidated financial statements.
In May 2017, the FASB issued ASU 2017-09, Compensation—Stock Compensation (Topic 718): Scope of Modification Accounting, which clarifies when an entity will apply modification accounting for changesrelated to stock-based compensation arrangements. Modification accounting applies if the value, vesting conditions, or classification of the awards changes. The ASU will be effective for annual periods beginning after December 15, 2017,large development and interim periods within those annual periods. Early adoption is permitted. The Company is currently evaluating the impact of adopting this guidance on its consolidated financial statements.
In March 2017, the FASB issued ASU 2017-07, Compensation—Retirement Benefits (Topic 715): Improving the Presentation of Net Periodic Pension Cost and Net Periodic Postretirement Benefit Cost, which requires entities to report the service cost component of the net periodic benefit costcommercial programs in the same income statement lineBiologics segment, such as other compensation costs arising frommanufacturing and development services renderedfor gene therapy offerings, where revenue is recorded over time and the ability to invoice customers is dictated by employees duringcontractual terms. As of December 31, 2023, the reporting period. The other components of the net benefit costs will be presented in the income statement separately from the service cost and below the income from operations subtotal. The ASU will be effective for public reporting entities in fiscal years beginning after December 15, 2017, and interim periods within those years. Early adoption is permitted in the first interim period of a fiscal year. The Company is currently evaluating the impact of adopting this guidance onrecorded no reserve against its consolidated financial statements.aggregate contract asset balance.
In January 2017, the FASB issued ASU 2017-01, Business Combinations (Topic 805): Clarifying the Definition of a Business, which provides additional guidance on the definition of a business to assist entities with evaluating whether transactions should be accounted for as acquisitions of assets or businesses. The ASU will be effective for public reporting entities in fiscal years beginning after December 15, 2017 and interim periods within those fiscal years. The Company is currently evaluating the impact of adopting this guidance on its consolidated financial statements.Performance Obligations
In February 2016, the FASB issued ASU 2016-02 Leases (Topic 842), which will supersede ASC 840 Leases. The new guidance requires lessees to recognize most leases on their balance sheets for the rights and obligations created by those leases. The guidance requires enhanced disclosures regarding the amount, timing and uncertainty of cash flows arising from leases and will be effective for publicly reporting entities in annual reporting periods beginning after December 15, 2018, and interim periods within those fiscal years. Early adoption is permitted. The guidance is required to be adopted using the modified retrospective approach. The Company anticipates that most of its operating leases will result in the recognition of additional assets and corresponding liabilities on its consolidated balance sheets. The Company continues to evaluate the impact of adopting this guidance and its implication on its consolidated financial statements.
In May 2014, the FASB issued ASU No. 2014-09Revenue from Contracts with Customers, whichwill supersede nearly all existing revenue recognition guidance. The new guidance’s core principle is that a company will recognize revenue when it transfers promised goods or services to customers in an amount that reflects the consideration to which the company expects to be entitled in exchange for those goods or services. In doing so, the new guidance creates a five-step model that requires a

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company to exercise judgment when considering the terms of the contracts and all relevant facts and circumstances. The five steps require a company to identify customer contracts, identify the separateRemaining performance obligations determine the transaction price, allocate the transaction price to the separate performance obligationsrepresent firm orders for future development services as well as manufacturing and recognize revenue when each performance obligation is satisfied. On July 9, 2015, the FASB approved a one-year deferral of the effective date so that the new guidance is effective for public entities for annual and interim periods beginning after December 15, 2017. The new guidance allows for either full retrospective adoption, where the standard is applied to all periods presented, or modified retrospective adoption where the standard is applied only to the most current period presented in the financial statements. Early adoption is permitted. The Company has identified its revenue streams, reviewed the initial impacts of adopting of the new standard on those revenue streams, and appointed a governance committee and project management leader. While the Company continues to assess all potential impacts of the standard, it has preliminarily assessed that the timing of revenue recognition may change for certain contractual arrangements containingcommercial product supply, including minimum volume commitments, infor which the price isthere are incomplete performance obligations for work not fixed or determinable pursuant to the termsyet completed under executed contracts. Remaining performance obligations as of the agreement. Under the current standard, the related pricing adjustments are considered to be contingent, while under the new standard they will likely be accounted for as variable consideration and revenue might be recognized earlier provided that the Company can reliably estimate the amount expected to be realized.  Further, the Company has preliminarily determined that, for commercial supply arrangements, revenue will be recognized at the point in time of completing the required quality assurance process.December 31, 2023 were $692 million. The Company expects to adoptrecognize approximately 36% of the new standard on a modified retrospective basis.remaining performance obligations in existence as of December 31, 2023 after June 30, 2024.
2.BUSINESS COMBINATIONS

Transaction Overview:3.    BUSINESS COMBINATIONS
OnMetrics Contract Services Acquisition

In October 23, 2017,2022, the Company acquired 100% of the equity interestMetrics Contract Services (“Metrics”) from Mayne Pharma Group Limited for $474 million in Cook Pharmica LLC (now doing business as Catalent Indiana, LLC, "Catalent Indiana") forcash. Metrics, based in Greenville, North Carolina, is an aggregate nominal purchase price of $950 million, subject to adjustment, in order to enhance the Company's biologics capabilities. Catalent Indiana is a biologics-focused contractoral solids development and manufacturing organization with capabilities across biologics development, clinicalbusiness specializing in the manufacture of drugs containing highly potent active pharmaceutical ingredients. The operations and commercial cell culture manufacturing, formulation, finished-dose manufacturing,facility acquired have become part of the Company’s Pharma and packaging.Consumer Health segment.


The Company accounted for the Metrics transaction using the acquisition method of accounting for business combinations, in accordance with ASC 805, Business Combinations. Combinations. The total consideration was (in thousands):
Cash paid at closing$748,002
Fair value of deferred consideration at closing 184,838
    Total consideration$932,840

In addition to the cash paid at the closingCompany funded this acquisition with a portion of the acquisition, the agreement governing the purchase includes a deferred consideration arrangement that requires the Company to payproceeds of an additional $200.0 million in $50.0 million increments on each of the first four anniversaries of the closing. The fair value of the deferred consideration recognized on the acquisition date was estimated by calculating the risk-adjusted present value of four deferred cash payments and includes a component of imputed interest. This deferred consideration is included in current and long-term obligations within the consolidated balance sheet at December 31, 2017.
Following the acquisition, the operating results of the Catalent Indiana business have been included in the consolidated financial statements. For the periodOctober 2022 drawdown from the acquisition date through December 31, 2017, Catalent Indiana's net revenue was $40.4 million and pre-tax earnings were $7.9 million. Transaction costs incurred as a result of the acquisition of $1.9 million and $10.4 million are included in selling, general and administrative expenses for the three and six months ending December 31, 2017, respectively.

Valuation Assumptions and Preliminary Purchase Price Allocation:

its senior secured revolving credit facility. The Company estimated fair values at the date of acquisition for the preliminary allocation of consideration to the net tangible and intangible assets acquired and liabilities assumed. During the measurement period, the Company will continue to obtain information to assist in finalizing the fair value of net assets acquired, which may differ materially from these preliminary estimates. If any measurement period adjustment is material, the Company will record those adjustments, including any related impact on net income, in the reporting period in which the adjustments are determined.


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The preliminary purchase price allocation to assets acquired and liabilities assumed in the transaction is (in thousands):as follows:


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Accounts Receivable$37,021
Inventory 25,144
Other current assets 1,344
Property, plant and equipment 221,139
Identifiable intangible assets 330,000
Trade and other payables 5,380
Deferred revenue 18,132
Total identifiable net assets 591,136
Goodwill 341,704
Total assets acquired and liabilities assumed$932,840

(Dollars in millions)Final Purchase Price Allocation
Trade receivables, net$15 
Inventories
Property, plant, and equipment195 
Other intangibles, net52 
Other, net(12)
Goodwill219 
Total assets acquired and liabilities assumed$474 
The carrying value of trade receivables, raw materials inventory, and trade payables, as well as certain other current and non-current assets and liabilities generally represented the fair value at the date of acquisition.

Property, plant and equipment was valued using a combinationOther intangibles, net consists of the sales comparison approach and cost approach,customer relationships of $52 million, which is based on current replacement and/or reproduction cost of the asset as new, less depreciation attributable to physical, functional, and economic factors. The Company then determined the remaining useful life based on the anticipated life of the asset and Company policy for similar assets.

Customer relationship intangible assets of $330 million were valued using the multi-period, excess-earnings method, a method that values the intangible asset using the present value of the after-tax cash flows attributable to the intangible asset only. The significant assumptions used in developing the valuation included the estimated annual net cash flows (including application of an appropriate margin to forecasted revenue, selling and marketing costs, return on working capital, contributory asset charges, and other factors), the discount rate whichthat appropriately reflects the risk inherent in each future cash flow stream, theand an assessment of the asset’s life cycle, as well as other factors. The assumptions used in the financial forecasts were based on historical data, supplemented by current and anticipated growth rates, management plans, and market comparablemarket-comparable information. Fair valueFair-value determinations require considerable judgment and are sensitive to changes in underlying assumptions and factors. Preliminary assumptions may change and may result in significant changes to the final valuation. The customer relationship intangible asset has a weighted average useful life of 1412 years.


Property, plant, and equipment was valued using the cost approach, which is based on current replacement and/or reproduction cost of the asset as new, less depreciation attributable to physical, functional, and economic factors. The Company then determined the remaining useful life based on the anticipated life of the asset and Company policy for similar assets.

Goodwill has preliminarily beenwas allocated to our Drug Delivery Solutions segment as shown in Note 3, the Pharma and Consumer Health segment. Goodwill. Goodwill is expected to be deductible for tax purposes and is mainly comprised of the following: growth from an expected increase in capacity utilization and potential new customers andcustomers. The goodwill resulting from the biologic expertise and know-how acquired with theMetrics acquisition of Catalent Indiana's workforce.is not deductible for tax purposes.


Pro Forma Results:

The following table provides unaudited pro forma results for the Company, prepared in accordance with ASC 805, for the three and six months ended December 31, 2017 and December 31, 2016, as if the Company had acquired Catalent Indiana as of July 1, 2016.
 For the Three Months Ended For the Six Months Ended
 December 31, 2017 December 31, 2016 December 31, 2017 December 31, 2016
 (in millions, except per share data)
Revenue$621.0
 $531.1
 $1,216.2
 $1,016.6
Net income/(loss)(10.5) 17.6  (1.0) (0.6)
Basic earnings/(loss) per share(0.08) 0.13  (0.01) 0.00 
Diluted earnings/(loss) per share(0.08) 0.13  (0.01) 0.00 

The unaudited pro forma financial information was prepared based on the historical information of Catalent and Catalent Indiana. In order to reflect the acquisition on July 1, 2016, the unaudited pro formal financial information includes adjustments

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to reflect the incremental amortization expense to be incurred based on the fair valueResults of the intangible assetsbusiness acquired the incremental depreciation expense relatedwere not material to the fair value adjustments associated with Catalent Indiana's property, plant and equipment, the additional interest expense associated with the issuanceCompany's consolidated statement of debt to finance the acquisition, the shares issued in connection with the first quarter equity offering to finance the acquisition, and the acquisition, integration, and financing-related costs incurred during the three and six months ended December 31, 2017 and 2016. The results do not include any anticipated cost savingsoperations, financial position, or other effects associated with integrating Catalent Indiana into the rest of the Company. Unaudited pro forma amounts are not necessarily indicative of results had the acquisition occurred on July 1, 2016 or of future results.cash flows.
3.GOODWILL
4.    GOODWILL
The following table summarizes the changes between June 30, 20172023 and December 31, 20172023 in the carrying amount of goodwill in total and by reporting segment:
(Dollars in millions)BiologicsPharma and Consumer HealthTotal
Balance at June 30, 2023$1,563 $1,476 $3,039 
Foreign currency translation adjustments(3)(1)
Impairment (1)
(392)(295)(687)
Balance at December 31, 2023$1,173 $1,178 $2,351 
(Dollars in millions)Softgel Technologies Drug Delivery Solutions Clinical Supply Services Total
Balance at June 30, 2017$415.2
 $477.2
 $151.7
 $1,044.1
Additions
 341.7
 
 341.7
Divestitures(0.9) 
 
 (0.9)
Foreign currency translation adjustments8.9
 8.3
 6.2
 23.4
Balance at December 31, 2017$423.2
 $827.2
 $157.9
 $1,408.3
The reduction in goodwill(1) Represents gross impairment charges in the Softgel Technologies reporting segment relates to the sale of two manufacturing sites in the Asia Pacific region. The site divestitures were neither material individually or in aggregate to the segment or to the Company. The increase inperiod. Accumulated goodwill in the Drug Delivery Solutions reporting segment relates to the Catalent Indiana acquisition. See note 2 Business Combinations. There were no impairment charges recorded in the current period.amount to $897 million.
4.DEFINITE LIVED LONG-LIVED ASSETS
The Company’s definite-lived long-lived assets include property, plant and equipment as well as other intangible assets with definite lives. Refer to Note 15 Supplemental Balance Sheet Information for details related to property, plant, and equipment.
The details of other intangible assets subject to amortization as of December 31, 2017 and June 30, 2017, are as follows:Goodwill Impairment Charges
19
(Dollars in millions)Weighted Average Life 
Gross
Carrying
Value
 
Accumulated
Amortization
 
Net
Carrying
Value
December 31, 2017       
Amortized intangibles:       
Core technology18 years $172.7
 $(81.2) $91.5
Customer relationships14 years 589.3
 (121.2) 468.1
Product relationships12 years 212.0
 (189.6) 22.4
Total intangible assets  $974.0
 $(392.0) $582.0
The increase in customer relationships is associated with the acquisition of Catalent Indiana in October 2017. Refer to Note 2 Business Combinations for details of the acquisition.
(Dollars in millions)Weighted Average Life 
Gross
Carrying
Value
 
Accumulated
Amortization
 
Net
Carrying
Value
June 30, 2017       
Amortized intangibles:       
Core technology18 years $170.3
 $(74.8) $95.5
Customer relationships14 years 253.0
 (106.1) 146.9
Product relationships12 years 206.9
 (176.2) 30.7
Total intangible assets  $630.2
 $(357.1) $273.1

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Amortization expenseAs a result of the Consumer Health reporting unit's underperformance of recent operating results relative to expectations, the current macroeconomic conditions impacting the consumer health and biotechnology industries, and increased interest rates, the Company assessed the current and future economic outlook as of September 30, 2023 for its reporting units in its Pharma and Consumer Health and Biologics segments and identified indicators for impairment of the goodwill previously recorded for two of its reporting units. The evaluation began with a qualitative assessment of the Company's Consumer Health and Biomodalities reporting units to determine if it was $16.1 millionmore likely than not that the fair value of the reporting units was less than its carrying value. The qualitative assessment did not indicate that it was more likely than not that the fair value exceeded the carrying value in its Consumer Health and 27.5 millionBiomodalities reporting units, which led to a quantitative assessment for the threecorresponding reporting units.

The Company estimated the fair value of its reporting units using a combination of the income and six months endedmarket approaches. In performing the goodwill impairment test, the Company used a terminal revenue growth rate of 3.5% and discount rates ranging from 9% to 10% in its estimation of fair value. The evaluation performed resulted in impairment charges of $687 million with respect to the Consumer Health and Biomodalities reporting units.
While the Company believes the assumptions it used were reasonable and commensurate with the views of a market participant, changes in key assumptions, including increasing the discount rate, lowering forecasts for revenue and operating margin or lowering the long-term growth rate could lead to the conclusion that an additional impairment was appropriate.
A qualitative assessment was performed as of December 31, 2017, respectively, and $11.1 million and $22.1 million for the three and six months ended December 31, 2016, respectively. Future amortization expense for the next five fiscal years is estimated to be:2023, which yielded no indicators of impairment.
20
(Dollars in millions)Remainder 
 Fiscal 2018
 2019 2020 2021 2022 2023
Amortization expense$34.8
 $63.8
 $49.7
 $49.7
 $49.7
 $49.7

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5.    LONG-TERM OBLIGATIONS AND SHORT-TERM BORROWINGS
5.LONG-TERM OBLIGATIONS AND OTHER SHORT-TERM BORROWINGS
Long-term obligations and other short-term borrowings consistconsisted of the following at December 31, 20172023 and June 30, 2017:2023:
(Dollars in millions)MaturityDecember 31, 2023June 30, 2023
Senior secured credit facilities
Term loan facility B-3 (7.471% as of December 31, 2023)February 2028$1,411 $1,418 
Term loan facility B-4 (8.356% as of December 31, 2023)February 2028600 — 
Revolving credit facilityNovember 2027— 500 
5.000% senior notes due 2027July 2027500 500 
2.375% Euro senior notes due 2028(1)
March 2028910 904 
3.125% senior notes due 2029February 2029550 550 
3.500% senior notes due 2030April 2030650 650 
Financing lease obligations2023 to 2038398 341 
Other obligations(2)
2023 to 202836 25 
Unamortized discount and debt issuance costs(50)(39)
Total debt$5,005 $4,849 
Less: current portion of long-term obligations and other short-term
     borrowings
46 536 
Long-term obligations, less current portion$4,959 $4,313 
(Dollars in millions)Maturity as of December 31, 2017 December 31, 
 2017
 June 30, 2017
Senior Secured Credit Facilities     
Term loan facility dollar-denominatedMay 2024 $1,234.9
 $1,244.2
       Term loan facility euro-denominatedMay 2024 366.5
 352.0
Euro-denominated 4.75% Senior Notes due 2024December 2024 445.4
 424.3
U.S. dollar-denominated 4.875% Senior Notes due 2026January 2026 443.7
 
Deferred purchase considerationSeptember 2021 186.0
 
$200 million revolving credit facilityMay 2022 
 
Capital lease obligations2020 to 2032 62.8
 53.3
Other obligations2018 to 2019 3.1
 5.9
Total  2,742.4
 2,079.7
Less: Current portion of long-term obligations and other short-term
borrowings
  69.9
 24.6
Long-term obligations, less current portion  $2,672.5
 $2,055.1
(1)    The change in the carrying value of this euro-denominated debt was due to fluctuations in foreign currency exchange rates.
Senior Secured Credit Facilities and Third Amendment(2)    The increase in other obligations is primarily associated with $15 million in proceeds from a failed sale-leaseback transaction that occurred in the three months ended September 30, 2023.
On October 18, 2017,November 22, 2023, Operating Company, completedentered into Amendment No. 310 (the "Third Amendment"“Tenth Amendment”) to its Amended and Restated Credit Agreement dated as of May 20, 2014 (as subsequently amended, the "Credit Agreement"“Credit Agreement”), governing the senior secured credit facilities that provide U.S. dollar denominated term loans, euro-denominated term loans and a revolving credit facility. The Third Amendment lowered the interest rate on U.S. dollar-denominated and euro-denominated term loans and the revolving credit facility and extended the maturity dates on the senior secured credit facilities by three years. The new applicable rate for U.S. dollar-denominated term loans is LIBOR (the London Interbank Offered Rate, subject to a floor of 1.00%) plus 2.25%, which Tenth Amendment further extends the deadlines by which the Operating Company is 0.50% lower thanrequired to deliver to the previous rate,administrative agent (i) its audited financial statements as at the end of and the new applicable rate for euro-denominated term loans is LIBOR (subject to a floor of 1.00%) plus 1.75%, which is 0.75% lower than the previous rate. The new applicable rate for the revolving loans is initially LIBOR plus 2.25%, which is 1.25% lower thanfiscal year ended June 30, 2023, together with the previous rate,auditor’s report and opinion on such rate can additionally be reducedaudited financial statements, to LIBOR plus 2.00% in future periods based on a measure of Operating Company's total leverage ratio. The term loans and revolving loans will now mature in MayJanuary 26, 2024, and May 2022, respectively. The Third Amendment also includes a prepayment(ii) its unaudited financial statements as at the end of 1.0% inand for the event of another repricing event on or before the six-month anniversary of the Third Amendment.fiscal quarter ending September 30, 2023 to March 13, 2024.
Euro-denominated 4.75% Senior Notes due 2024
On December 9, 2016,19, 2023, Operating Company completed a private offering of €380.0entered into Amendment No. 11 (the “Eleventh Amendment”) to the Credit Agreement. Pursuant to the Eleventh Amendment, the Operating Company incurred $600 million aggregate principal amount of 4.75% Senior Notes due 2024U.S. dollar-denominated term B-4 loans (the "Euro Notes"“Term B-4 Loans”).The Term B-4 Loans are a new class of term loans under the Credit Agreement, with an interest rate, at Operating Company’s option, of either (i) the term SOFR rate plus 3.00% or (ii) the base rate plus 2.00%; provided, that the term SOFR rate shall not be less than 0.50%. The Euro Notes are fullyTerm B-4 Loans have a maturity date of February 2028, quarterly amortization of principal equal to 1.00% with payments on the last business day of March, June, September, and unconditionally guaranteed, jointly and severally, by all of the wholly owned U.S. subsidiaries of Operating Company that guarantee its senior secured credit facilities.December. The Euro Notes were offered in the United States to qualified institutional buyers in reliance on Rule 144A under the Securities Act and outside the United States only to non-U.S. investors pursuant to Regulation S under the Securities Act. The Euro Notes will mature on December 15, 2024, bear interest at the rate of 4.75% per annum and are payable semi-annually in arrears on June 15 and December 15 of each year.

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U.S. Dollar-denominated 4.875% Senior Notes due 2026
On October 18, 2017, Operating Company completed a private offering (the "Debt Offering") of $450.0 million aggregate principal amount of 4.875% senior unsecured notes due 2026 (the "USD Notes"). The USD Notes are fully and unconditionally guaranteed, jointly and severally, by all of the wholly owned U.S. subsidiaries of Operating Company that guarantee its senior secured credit facilities. The USD Notes were offered in the United States to qualified institutional buyers in reliance on Rule 144A under the Securities Act and outside the United States only to non-U.S. investors pursuant to Regulation S under the Securities Act. The USD Notes will mature on January 15, 2026, bear interest at the rate of 4.875% per annum, and are payable semi-annually in arrears on January 15 and July 15 of each year, beginning on July 15, 2018. The net proceeds of the Debt Offering,Term B-4 Loans, after payment of the initial purchasers' discount and related fees and expenses, were used to fund a portionrepay the existing Revolving Credit Facility under the Credit Agreement, plus accrued and unpaid interest thereon.

21

Table of the consideration for the Catalent Indiana acquisition due at its closing.Contents
Deferred Purchase Consideration
In connection with the acquisition of Catalent Indiana in October 2017, $200 million of the $950 million aggregate nominal purchase price is payable in $50 million installments, on each of the first four anniversaries of the closing date. The deferred purchase consideration is recorded at fair value and includes a component of imputed interest.
Bridge Loan Facility
On September 18, 2017, contemporaneous with the Company entering into the agreement to acquire Catalent Indiana, Operating Company entered into a debt commitment letter with Morgan Stanley Senior Funding, Inc., JP Morgan Chase Bank, N.A., Royal Bank of Canada, RBC Capital Markets, Bank of America, N.A. and Merrill Lynch, Pierce, Fenner & Smith Incorporated, as commitment parties. Pursuant to the debt commitment letter and subject to its terms and conditions, the commitment parties agreed to provide a senior unsecured bridge loan facility (the "Bridge Facility") of up to $700.0 million in the aggregate for the purpose of providing any back-up financing necessary to fund a portion of the consideration to be paid in the acquisition and related fees, costs and expenses (the "Bridge Loan Commitment"). In connection with entering into the Bridge Facility, Operating Company incurred $6.1 million of associated fees, which was recorded in prepaid expenses and other in the consolidated balance sheet as of September 30, 2017. Operating Company did not draw on it to fund the acquisition and the Company expensed the $6.1 million in the second quarter as part of other income and expense and the facility was closed. See Note 7 for further discussion of financing costs incurred in the second quarter.
Debt Covenants
Senior Secured Credit Facilities
The Revolving Credit Agreement contains a number of covenants that, among other things, restrict, subject to certain exceptions, Operating Company’s (and Operating Company’s restricted subsidiaries’) ability to incur additional indebtedness or issue certain preferred shares; create liens on assets; engage in mergers and consolidations; sell assets; pay dividends and distributions or repurchase capital stock; repay subordinated indebtedness; engage in certain transactions with affiliates; make investments, loans or advances; make certain acquisitions; enter into sale and leaseback transactions; amend material agreements governing Operating Company’s subordinated indebtedness; and change Operating Company’s lines of business.
The Credit Agreement also contains change of control provisions and certain customary affirmative covenants and events of default. The revolving credit facilityFacility requires compliance with a net leverage covenant when there is a 30% or more draw outstanding at a period end. As of December 31, 2017, Operating Company was2023, we were in compliance with all material covenants related to its long-term obligations.
Subject to certain exceptions,under the Credit Agreement permits Operating Company and its restricted subsidiariesAgreement.

In addition to incur certain additional indebtedness, including secured indebtedness. Noneoutstanding borrowings under the Revolving Credit facility, the available capacity under the Revolving Credit Facility is further reduced by the aggregate value of Operating Company’s non-U.S. subsidiaries or Puerto Rico subsidiaries is a guarantorall outstanding letters of the loans.
Undercredit under the Credit Agreement, Operating Company’s ability to engage in certain activities such as incurring certain additional indebtedness, making certain investments and paying certain dividends is tied to ratios based on Adjusted EBITDA (which is defined as “Consolidated EBITDA” in the Credit Agreement). Adjusted EBITDA is based on the definitions in the Credit Agreement, is not defined under U.S. GAAP, and is subject to important limitations.
The Euro Notes and the USD Notes
The Indentures governing the Euro Notes and the USD Notes (the "Indentures") contain certain covenants that, among other things, limit the ability of Operating Company and its restricted subsidiaries to incur or guarantee more debt or issue certain preferred shares, pay dividends on, repurchase or make distributions in respect of their capital stock or make other

19



restricted payments, make certain investments, sell certain assets, create liens, consolidate, merge, sell or otherwise dispose of all or substantially all of their assets, enter into certain transactions with their affiliates, and designate their subsidiaries as unrestricted subsidiaries. These covenants are subject to a number of exceptions, limitations and qualifications as set forth in the Indentures. The Indentures also contain customary events of default including, but not limited to, nonpayment, breach of covenants, and payment or acceleration defaults in certain other indebtedness of Operating Company or certain of its subsidiaries. Upon an event of default, either the holders of at least 30% in principal amount of each of the then-outstanding Euro Notes or the then-outstanding USD Notes, or either of the Trustees under the Indentures, may declare the applicable notes immediately due and payable, or in certain circumstances, the applicable notes will become automatically immediately due and payable.Agreement. As of December 31, 2017,2023, Operating Company was in compliance with all material covenantshad $1.09 billion of available capacity under the Indentures.Revolving Credit Facility, due to $6 million of outstanding letters of credit.
Measurement of the Estimated Fair Value of Debt Instruments

The estimated fair value of the Company’s senior secured credit facility,facilities and other senior indebtedness is classified as a Level 2 determination (see Note 10, Fair Value Measurements to our consolidated financial statements, for a description of the method by which fair value estimate,classifications are determined) in the fair-value hierarchy and is based on the quotedcalculated by using a discounted cash flow model with a market prices for the same or similar issues or on the current rates offered for debt of the same remaining maturities and considers collateral, if any. The estimated fair value of the Euro and USD Notes,interest rate as a Level 1 fair value estimate, is based on the quoted market prices of the instruments.significant input. The carrying amounts and the estimated fair values of financial instrumentsthe Company’s principal categories of debt as of December 31, 20172023 and June 30, 20172023 are as follows:

December 31, 2023June 30, 2023
(Dollars in millions)Fair Value Measurement
Carrying
Value
Estimated Fair
Value
Carrying
Value
Estimated Fair
Value
5.000% senior notes due 2027Level 2$500 $499 $500 $482 
2.375% Euro senior notes due 2028Level 2910 836 904 784 
3.125% senior notes due 2029Level 2550 508 550 481 
3.500% senior notes due 2030Level 2650 598 650 566 
Senior secured credit facilities & otherLevel 22,445 2,225 2,284 2,141 
Subtotal$5,055 $4,666 $4,888 $4,454 
Unamortized discount and debt issuance
   costs
(50)— (39)— 
Total debt$5,005 $4,666 $4,849 $4,454 

6.    (LOSS) EARNINGS PER SHARE
  December 31, 2017 June 30, 2017
(Dollars in millions)Fair Value Measurement
Carrying
Value
 
Estimated Fair
Value
 
Carrying
Value
 
Estimated Fair
Value
Euro-denominated 4.75% Senior NotesLevel 1$445.4
 $474.4
 $424.3
 $454.0
U.S. Dollar-denominated 4.875% Senior NotesLevel 1443.7
 449.8
 
 
Senior Secured Credit Facilities & OtherLevel 21,853.3
 1,825.1
 1,655.4
 1,653.1
Total $2,742.4
 $2,749.3
 $2,079.7
 $2,107.1
6.EARNINGS PER SHARE
The Company computes (loss) earnings per share of the Company’s common stock, par value $0.01 (the “Common Stock”) using the treasury stock method. Diluted net (loss) earnings per share is computed using the weighted average number of shares of Common Stock outstanding plus the weighted average number of shares of Common Stock that would be issued assuming exercise or conversion of all potentially dilutive instruments. Dilutive securities having an anti-dilutive effect on diluted net earnings per share are excluded from the calculation. The dilutive effect of the securities that are issuable under the Company’s equity incentive plans are reflected in diluted earnings per share by application of the treasury stock method. The reconciliations between basic and diluted earnings per share attributable to Catalent common shareholders for the three and six months ended December 31, 20172023 and 2016,2022, respectively, are as follows (in millions, except share and per share data):follows:

Three Months Ended  
December 31,
Six Months Ended  
December 31,
(In millions except per share data)2023202220232022
Net (loss) earnings$(206)$81 $(965)$81 
Weighted average shares outstanding - basic182 181 181 180 
Weighted average dilutive securities issuable - stock plans— — — 
Weighted average shares outstanding - diluted182 181 181 181 
(Loss) earnings per share: 
Basic$(1.13)$0.45 $(5.31)$0.45 
Diluted$(1.13)$0.44 $(5.31)$0.45 

22

 Three Months Ended  
 December 31,
 Six Months Ended  
 December 31,
 2017 2016 2017 2016
Net earnings/(loss)$(21.9) $17.4
 $(18.1) $22.0
        
Weighted average shares outstanding132,983,262
 124,889,681
 129,327,188
 124,870,327
Dilutive securities issuable-stock plans
 1,524,963
 
 1,470,476
Total weighted average diluted shares outstanding132,983,262
 126,414,644
 129,327,188
 126,340,803
        
Basic earnings per share of common stock:   
    
Net earnings/(loss)$(0.16) $0.14
 $(0.14) $0.18
        
Diluted earnings per share of common stock:       
Net earnings/(loss)$(0.16) $0.14
 $(0.14) $0.17
The computation of diluted earnings per shareShares with an antidilutive effect on the weighted average shares outstanding for the three and six months ended December 31, 2017 excludes the maximum effect of the potential common shares issuable under the employee stock option plan of approximately 2.6 million shares,2023 and excludes restricted share awards of 2.1 million shares, because the Company had a net loss for the period and the effect would therefore be anti-dilutive. The computation of diluted earnings per share for the three and six months ended December 31, 2016 excludes the effect of 0.5 million shares potentially issuable pursuant to awards granted under the 2007 Stock Incentive Plan, because the vesting provisions of those awards specify performance- or market-based conditions that had2022 were not been met as of the period end. The computation of diluted earnings per share for the three and six months ended December 31, 2016 excludes the effect of potential common shares issuable under employee-held stock options and restricted stock units of approximately 0.9 million and 1.1 million shares, respectively, because they are anti-dilutive.material.

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7.    OTHER EXPENSE (INCOME), NET

7.OTHER (INCOME)/EXPENSE, NET
The components of other expense (income)/expense,, net for the three and six months ended December 31, 20172023 and 20162022 are as follows:
Three Months Ended  
December 31,
Six Months Ended 
December 31,
(Dollars in millions)2023202220232022
Foreign currency losses (gains) (1)
$$(25)15 (1)
     Other— 
Total other expense (income), net$$(23)$17 $

(1)    Foreign currency remeasurement gains/losses include both cash and non-cash transactions.
8.     RESTRUCTURING COSTS
 Three Months Ended  
 December 31,
 Six Months Ended 
 December 31,
(Dollars in millions)2017 2016 2017 2016
Other (income)/expense, net       
Debt refinancing costs (1)
$11.8
 $4.3
 $11.8
 $4.3
Foreign currency (gains) and losses1.3
 (5.3) 6.9
 (7.5)
     Other0.5
 (0.8) 0.6
 (0.7)
Total other (income)/expense, net$13.6
 $(1.8) $19.3
 $(3.9)
(1) The 2017 debt refinancing costs include financing charges relatedFrom time to time, the offering of the USD Notes and the Third Amendment and also include a $6.1 million charge for commitment fees paid during the first quarter of fiscal 2018 on the Bridge Facility. The 2016 debt refinancing costs include financing charges of $4.3 million related to the December 2016 offering of the Euro Notes and repricing and partial paydown of the Company's term loans.
8.RESTRUCTURING AND OTHER COSTS
Restructuring Costs
The Company has implementedimplements plans to restructure certain operations, both domestically and internationally. The restructuring plans focused on various aspects of operations, including, among others, closing and consolidating certain manufacturing operations, rationalizing headcount and aligning operations in a strategic and more cost-efficient structure. In addition, the Company may incur restructuring charges in the future in cases where a material change in the scope of operation with its business occurs. Employee-related restructuring costs consist primarily of severance costs and also include outplacement services provided to employees who have been involuntarily terminated and duplicate payroll costs during transition periods. Facility exit and other such restructuring costs consist of accelerated depreciation, equipment relocation costs and costs associated with planned facility expansions and closures to streamline Company operations.
Other Costs / (Income)During the fiscal year ended June 30, 2023, the Company adopted plans to reduce costs, consolidate facilities, and optimize its infrastructure across the organization. During the three months ended December 31, 2023, the Company extended its restructuring efforts to reduce costs and headcount in both its Biologics and Pharma and Consumer Health segments.
Other income includes settlementIn October 2023, and in connection with the Company's restructuring plans, the Company committed to a plan to close operations at its San Francisco facility and to transfer those operations to other sites within its network. The Company expects to incur cash and non-cash charges net of any insurance recoveries related toat least $25 million in connection with the probable resolution of certain customer claimssite closure, primarily related to a previous temporary suspensionpension liability from a multi-employer pension plan and accelerated depreciation of operations at a softgel manufacturing facility. Refer to Note 13 Commitmentsproperty, plant and Contingenciesequipment in the second half of fiscal 2024. Results for further discussionsthe three months ended December 31, 2023 are reflected in the tables below under the Pharma and Consumer Health segment.
In connection with these restructuring plans, the Company reduced its headcount by approximately 300 employees and incurred cumulative employee-related charges of such claims.approximately $12 million, primarily associated with cash severance programs through December 31, 2023.
Restructuring costs for the three and six months ended December 31, 2023 and 2022 were recorded in Other Operating Expense in the Consolidated Statement of Operations.
The following table summarizes the significant costscharges recorded within restructuring costs:
Three Months Ended  
December 31,
Six Months Ended 
December 31,
(Dollars in millions) 
2023202220232022
Restructuring costs:  
       Employee-related reorganization$10 $12 $12 $14 
       Facility exit and other costs11 13 
Total restructuring costs$17 $23 $19 $27 
The following table summarizes the charges recorded within restructuring costs by segment. These amounts are excluded from Segment EBITDA as described in Note 15, Segment Information.
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 Three Months Ended  
 December 31,
 Six Months Ended 
 December 31,
(Dollars in millions) 
2017 2016 2017 2016
Restructuring costs:       
Employee-related reorganization$1.6
 $(0.1) $3.3
 $0.7
Facility exit and other costs(0.7) 0.2
 (0.2) 0.5
Total restructuring costs$0.9
 $0.1
 $3.1
 $1.2
Other - customer claims net of insurance recoveries(0.8) 3.2
 (1.8) 3.2
Total restructuring and other costs$0.1
 $3.3
 $1.3
 $4.4
Three Months Ended  
December 31,
Six Months Ended 
December 31,
(Dollars in millions) 
2023202220232022
Restructuring costs:
Biologics$$18 $$18 
Pharma and Consumer Health10 11 
Non-segment (Corporate)
Total restructuring costs$17 $23 $19 $27 

The following tables summarizes the change in the employee separation-related liability associated with the restructuring plans.

Employee-related restructuring
9.
(Dollars in millions)
DERIVATIVE INSTRUMENTS AND HEDGING ACTIVITIES
Balance, June 30, 2023$19 
Charges12 
Payments(15)
Balance, December 31, 2023$16 
9.    DERIVATIVE INSTRUMENTS AND HEDGING ACTIVITIES
Risk Management Objective of Using Derivatives
The Company is exposed to fluctuations in the currency exchange rates applicable exchange rate onto its investments in foreign operations.operations outside the U.S. While the Company does not actively hedge against changes in foreign currency, the Company has mitigated its exposure from its investments in its European operations by denominating a portion of its debt in euros. At December 31, 2017,2023, the Company had euro-denominated debt outstanding of $811.9$910 million that (U.S. dollar equivalent), which is designated and qualifies as a hedge of aagainst its net investment in foreignits European operations. For non-derivatives designated and qualifying as net investment hedges, the effective portionsportion of the translation gains or losses are reported in accumulated other comprehensive income/(loss)loss as part of the cumulative translation adjustment. The ineffective portions of the translation gains or losses are reported in the statement of operations. The following table includessummarizes net investment hedge activity during the three and six months ended December 31, 20172023 and December 31, 2016.2022.

Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)2023202220232022
Unrealized foreign exchange loss within other comprehensive income$(38)$(85)$(6)$(4)
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 Three Months Ended  
 December 31,
 Six Months Ended  
 December 31,
(Dollars in millions)2017 2016 2017 2016
Unrealized foreign exchange gain/(loss) within other
     comprehensive income
$(3.9) $13.6
 $(21.5) $10.0
Unrealized foreign exchange gain/(loss) within statement
     of operations
$(2.8) $10.2
 $(16.2) $7.6
The net accumulated gain ofon the instrument designated as thea hedge as of December 31, 20172023 within other comprehensive income/(loss)loss was approximately $38.5$91 million. Amounts are reclassified out of accumulated other comprehensive income/(loss)loss into earnings when the entity to which the gains and losses relate is either sold or substantially liquidated.
10.INCOME TAXES
Interest-Rate Swap
U.S. Tax Reform

On December 22, 2017,In February 2021, the U.S. government enacted wide-ranging tax legislation,Company entered into an interest-rate swap agreement with Bank of America N.A. (the “2021 Rate Swap”) as a hedge against the Tax Cuts and Jobs Act (the "2017 Tax Act"). The 2017 Tax Act significantly revises U.S. tax law by, among other provisions, (a) lowering the applicable U.S. federal statutory income tax rate from 35% to 21%, (b) creatingeconomic effect of a partial territorial tax system that includes imposing a mandatory one-time transition tax on previously deferred foreign earnings, (c) creating provisions regarding the (1) Global Intangible Low Tax Income ("GILTI"), (2) the Foreign Derived Intangible Income ("FDII") deduction, and (3) the Base Erosion Anti-Abuse Tax ("BEAT"), and (d) eliminating or reducing certain income tax deductions, such as interest expense, executive compensation expenses and certain employee expenses.

ASC 740 Income Taxes requires the effects of changes in tax laws to be recognized in the period in which the legislation is enacted. However, due to the complexity and significanceportion of the 2017 Tax Act’s provisions,variable interest obligation associated with its Term B-3 Loans. The 2021 Rate Swap effectively fixed the SEC staff issued Staff Accounting Bulletin No. 118 ("SAB 118"), which allows companies to record the tax effectsrate of interest payable on that portion of the 2017 Tax ActTerm B-3 Loans, thereby reducing the impact of future interest rate changes on a provisional basis based on a reasonable estimate and then, if necessary, subsequently adjust such amounts during a limited measurement period as more information becomes available. The measurement period ends when a company has obtained, prepared, and analyzed the information necessary to finalize its accounting, but cannot extend beyond one year from enactment.future interest expense. As a result of the 2017 Tax Act, 2021 Rate Swap, the variable portion of the applicable interest rate on $500 million of the Term B-3 Loans is now effectively fixed at 0.9985%.
To conform with the adoption of Topic 848, Reference Rate Reform and the Eighth Amendment, the Company revised its estimated annual effectiveamended the 2021 Rate Swap in June 2023 (the “2023 Rate Swap”). The 2023 Rate Swap continues to effectively fix the rate of interest payable on the same portion of our U.S. dollar-denominated term loans under our senior secured credit facilities. As a result of
24

the 2023 Rate Swap, the variable portion of the applicable interest rate on $500 million of the U.S. dollar-denominated term loans is now effectively fixed at 0.9431%.
The 2023 Rate Swap continues to reflectqualify for a cash-flow hedge. The Company evaluates hedge effectiveness at the inception of the hedge and on an ongoing basis. The cash flows associated with the 2023 Rate Swap amendment is reported in cash provided by operating activities in the consolidated statements of cash flows. The unrealized loss recorded in stockholder's equity related to the mark-to-market change in the U.S. federal statutory rate. The revised blended U.S. federal statutory tax rate for2021 Rate Swap during the fiscal year is 28%.

Measurement of certain income tax effects that can be reasonably estimated (provisional amounts)
During the second quarterthree and six months ended December 31, 2017, the Company recorded a one-time net charge of $46.0 million within its income tax provision as a provisional estimate2023 was $2 million.
A summary of the net accounting impactestimated fair value of the 2017 Tax Act2021 Rate Swap reported in accordance with SAB 118. The net chargethe consolidated balance sheets is comprised ofstated in the following: (i) expense of $48.7 million relatedtable below:
December 31, 2023June 30, 2023
(Dollars in millions)Balance Sheet ClassificationEstimated Fair ValueBalance Sheet ClassificationEstimated Fair Value
Interest-rate swapOther long-term assets$59 Other long-term assets$62 

10. FAIR VALUE MEASUREMENTS
ASC 820, Fair Value Measurement, defines fair value as the exit price that would be received to the mandatory transition tax for deemed repatriation of deferred foreign income, $8.7 million of which the Company expectssell an asset or paid to pay overtransfer a liability. Fair value is a market-based measurement that should be determined using assumptions that market participants would use in pricing an 8-year period after consideringasset or liability. Valuation techniques used to measure fair value should maximize the use of certain net operating lossesobservable inputs and foreign tax credits,minimize the use of unobservable inputs. To measure fair value, the Company uses the following fair value hierarchy based on three levels of inputs, of which Level 1 and certain limitations on executive compensation; (ii) an additional $9.5 million charge relatingLevel 2 are considered observable and Level 3 is considered unobservable:
Level 1 – Quoted prices in active markets for identical assets or liabilities.                      
Level 2 – Inputs other than Level 1 that are observable for the asset or liability, either directly or indirectly, such as quoted prices for similar assets and liabilities in active markets; quoted prices for identical or similar assets or liabilities in markets that are not active; or other inputs that are observable or can be corroborated by observable market data by correlation or other means.                      
Level 3 – Unobservable inputs that are supported by little or no market activity and that are significant to the impactfair value of provisional changesthe assets or liabilities. Value is determined using pricing models, discounted cash flow methodologies, or similar techniques and also includes instruments for which the determination of fair value requires significant judgment or estimation.
Assets and Liabilities Measured at Fair Value on a Recurring Basis
The carrying amounts of cash and cash equivalents, accounts receivable, accounts payable and accrued expenses of the Company approximate fair value based on the short maturities of these instruments.
The Company evaluates its financial assets and liabilities subject to fair value measurements on a recurring basis to determine the appropriate level of classification as of the end of each reporting period. The following table sets forth the Company’s financial assets and liabilities that were measured at fair value on a recurring basis and the fair value measurement for such assets and liabilities at December 31, 2023 and June 30, 2023:

25

(Dollars in millions)Basis of Fair Value Measurement
December 31, 2023TotalLevel 1Level 2Level 3
Assets:
Interest-rate swap$59 $— $59 $— 
Trading securities— — 
June 30, 2023
Assets:
Interest-rate swap$62 $— $62 $— 
Trading securities— — 
The fair value of the 2021 Rate Swap was determined, and the fair value of the 2023 Rate Swap will be determined, at the end of each reporting period based on valuation models that use interest rate yield curves and discount rates as inputs. The discount rates are based on U.S. deposit or U.S. Treasury rates. The significant inputs used in the Company's intentions with respect to future repatriation of undistributed earningsvaluation models are readily available in public markets or can be derived from non-U.S. subsidiariesobservable market transactions, and (iii) a benefit of $12.2 million related to a revaluation of the Company’s deferred tax assetsvaluation is therefore classified as Level 2 in the fair-value hierarchy.
Assets and liabilities. The one-time net charge, which was recordedLiabilities Measured at Fair Value on a provisional basis, increasedNon-Recurring Basis

Long-lived assets, goodwill, and other intangible assets are subject to non-recurring fair value measurement for the Company’s effective tax rate by 164% and 154%evaluation of potential impairment. There was no non-recurring fair value measurement during the three-month and six-month periodssix months ended December 31, 2017, respectively.2023.
Given the significant complexity of the 2017 Tax Act, anticipated guidance from the U.S. Treasury concerning implementation of the 2017 Tax Act, and the potential for additional guidance from the SEC or the FASB related to the 2017 Tax Act, the provisional estimates that the Company recorded may require adjustment during the measurement period. The provisional estimates were based on the Company’s present understanding of the 2017 Tax Act and other information available as of the time of the estimates, including assumptions and expectations about future events, such as its projected financial performance, and are subject to further refinement as additional information becomes available (including the Company’s actual full fiscal 2018 results of operations, as well as potential new or interpretative guidance issued by the SEC, the FASB, or the Internal Revenue Service) and the Company continues its analysis. The Company continues to analyze the changes to certain income tax deductions, assess calculations of earnings and profits in certain foreign subsidiaries, including whether those earnings are held in cash or other assets, and gather additional data to compute the full impact of the 2017 Tax Act on the Company’s deferred and current tax assets and liabilities.

11.    INCOME TAXES

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Measurement of certain income tax effects that cannot be reasonably estimated
Because of the complexity of the new GILTI tax rules, the Company continues to evaluate this provision of the 2017 Tax Act and the application of ASC 740. In accordance with ASC 740, the Company will make an accounting policy election of either (1) treating taxes due on future U.S. inclusions in taxable income related to GILTI as a current-period expense when incurred (the “period cost method”) or (2) factoring such amounts into the Company's measurement of its deferred taxes (the “deferred method”). The Company's selection of an accounting policy with respect to the new GILTI tax rules will depend, in part, on analyzing its global income to determine whether it expects to have future U.S. inclusions in taxable income related to GILTI and, if so, what the impact is expected to be. Whether the Company expects to have future U.S. inclusions in taxable income related to GILTI depends on not only the Company's current structure and estimated future results of global operations, but also its intent and ability to modify its structure. Therefore, the Company has not made any adjustment related to potential GILTI tax in its financial statements and has not made a policy decision regarding whether to record deferred tax on GILTI.

Additionally, the Company continues to evaluate the potential impact of all other provisions, including but not limited to provisions regarding the FDII, BEAT, interest expense and certain employee expense deductions, as well as the state tax impact of the 2017 Tax Act. The Company is currently in the process of analyzing its structure and estimated future results and, as a result, is not yet able to reasonably estimate the effect of these provisions of the 2017 Tax Act.

Other Tax Matters

The Company accounts for income taxes in accordance with ASC 740.740, Income Taxes. Generally, fluctuations in the effective tax rate are primarily due to changes in relative amounts of U.S. and non-U.S. pretax income, resulting from the Company’s business mix and changes in the tax impact of special items, and other discrete tax items, which may have unique tax implications depending on the nature of the item. Such discreteitems. Discrete items include, but are not limited to, changes in foreignnon-U.S. statutory tax rates, the amortization of certain assets, changes in the Company’s reserve for uncertain tax positions, and the tax impact of changes in its ASC 740 unrecognized tax benefit reserves. certain equity compensation.

In the normal course of business, the Company is subject to examination by taxing authorities around the world, including such majorworld. The Company is presently under audit in select jurisdictions asin the United States Germany, France, and in Europe, but no material impact is expected to the United Kingdom. The Company is no longer subject to new non-U.S.financial results once these audits are completed.

ASC 740 provides guidance for the accounting of uncertain income tax examinations for years prior to fiscal year 2008. Under the terms of the 2007 purchase agreement by which the selling stockholders acquired their interest in the Company, the Company is indemnified by its former owner for tax liabilities that may arise after the 2007 purchase that relate to tax periods prior to April 10, 2007. The indemnification agreement applies to, among other taxes, any and all federal, state and international income-based taxes as well as related interest and penalties. As of December 31, 2017 and June 30, 2017, approximately $0.7 million and $0.8 million, respectively, of unrecognized tax benefit are subject to indemnification by the Company's former owner.

ASC 740 includes guidance on the accounting for uncertainty in income taxespositions recognized in the financial statements.Company's tax filings. This standardguidance provides that a tax benefit from an uncertain tax position may be recognized when it is more likely than not that, based on technical merits, the position will be sustained upon examination, including resolution of any related appeal or litigation process, based on the technical merits.process. As of December 31, 2017, the Company had a total of $52.5 million of unrecognized tax benefits. A reconciliation of its reserves for uncertain tax positions, excluding accrued interest and penalties, for December 31, 2017 is as follows:
(Dollars in millions) 
Balance at June 30, 2017$52.5
Additions for tax positions of current year
Balance at December 31, 2017$52.5
As of December 31, 20172023 and June 30, 2017,2023, the Company had a total of $57.5 million and $57.5 million, respectively, ofCompany’s reserve against uncertain income tax positions (including accrued interest and penalties). As of these dates, $41.4 million and $41.4 million, respectively, represent the amount of unrecognized tax benefits, which, if recognized, would favorably affect the effective income tax rate. The Company recognizes interestremained substantially unchanged at $4 million. Interest and penalties related to uncertain tax positions are recognized as a component of income tax expense. As of

The Company recorded a provision for income taxes for the three months ended December 31, 20172023 of $24 million relative to loss before income taxes of $182 million. The Company recorded a provision for income taxes for the three months ended December 31, 2022 of $33 million relative to earnings before income taxes of $114 million. The income tax expense for the quarter is primarily the result of income tax expense in select international jurisdictions and June 30, 2017, the inability to recognize income tax benefit on incremental domestic losses. The quarterly provision was also impacted by the geographic distribution of the Company's pretax loss resulting from our business mix, changes in the tax impact of permanent differences, restructuring, special items, certain equity related compensation, and other discrete tax items that may have unique tax implications depending on the nature of the item.

The Company has approximately $5.0recorded a benefit for income taxes for the six months ended December 31, 2023 of $14 million relative to loss before income taxes of $979 million. The Company recorded a provision for income taxes for the six months ended December 31, 2022 of $36 million relative to earnings before income taxes of $117 million. The income tax benefit for the period is primarily the result of income tax expense in select international jurisdictions and $5.0 million, respectively, of accrued interest and penalties relatedthe inability to uncertainrecognize income tax positions. As of these dates, the portion of such interest and penalties subject to indemnification by its former owner is $1.5 million and $1.7 million, respectively.benefit on incremental domestic losses.


23
26


The year to date benefit was also impacted by the geographic distribution of the Company's pretax loss resulting from our business mix, changes in the tax impact of permanent differences, restructuring, special items, certain equity related compensation, and other discrete tax items that may have unique tax implications depending on the nature of the item.
11.EMPLOYEE RETIREMENT BENEFIT PLANS
12.    EMPLOYEE RETIREMENT BENEFIT PLANS
Components of the Company’s net periodic benefit costs are as follows:
Three Months Ended  
 December 31,
 Six Months Ended  
 December 31,
Three Months Ended
December 31,
Three Months Ended
December 31,
Six Months Ended  
December 31,
(Dollars in millions)2017 2016 2017 2016(Dollars in millions)2023202220232022
Components of net periodic benefit cost:       
Selling, general, and administrative expenses:
Selling, general, and administrative expenses:
Selling, general, and administrative expenses:
Service cost$0.9
 $0.8
 $1.8
 $1.6
Service cost
Service cost
Other operating expense:
Settlement charges
Settlement charges
Settlement charges
Other expense, net:
Interest cost
Interest cost
Interest cost1.8
 1.6
 3.6
 3.3
Expected return on plan assets(2.9) (2.6) (5.8) (5.4)
Amortization (1)
0.6
 1.0
 1.2
 2.1
Net amount recognized$0.4
 $0.8
 $0.8
 $1.6
(1)Amount represents the amortization of unrecognized actuarial gains/(losses).
(1) Amount represents the amortization of unrecognized actuarial losses.
As previously disclosed, the Company notified the trustees of a multi-employer pension plan of its withdrawal from participation in such plan in fiscal 2012. The actuarial review process administered by the plan trustees ended in fiscal 2015. For the three months ended December 31, 2023, the Company decided to withdraw its participation from a multi-employer pension plan as a result of recent restructuring activities in its Pharma and Consumer Health segment. The liabilityliabilities reported reflectsreflect the present value of the Company'sCompany’s expected future long-term obligations. The estimated discounted value of the projected contributions related to such plans was $39.1$44 million as of December 31, 20172023 and $38 million as of June 30, 20172023, and is included within pension liability on the consolidated balance sheets. The annual cash impact associated with the Company's obligationCompany’s obligations in such plan approximates $1.7is approximately $2 million.
The Company is in the process of terminating the U.S. pension plan and will settle with its participants either in a lump sum payout or through the purchase of an annuity contract, dependent upon the participant’s selection of payment. The Company will seek to purchase nonparticipating annuities for participants who do not elect lump sum payouts. Participants who elected a lump sum payout were settled in the three months ended December 31, 2023. The $7 million per year.of lump sum payments were made with cash from the assets of the qualified pension plan.
The Company performed an actuarial valuation analysis as of December 31, 2023 assuming the pension plan would be terminated through the purchase of non-participating group annuity contracts by March 31, 2024. The Company estimates a total settlement loss of $12 million, in which $3 million was recorded during the three months ended December 31, 2023. The estimated loss to settle the U.S. pension plan as of December 31, 2023 was based upon a 4.5% discount rate.
12.EQUITY AND ACCUMULATED OTHER COMPREHENSIVE INCOME/(LOSS)
13.    EQUITY AND ACCUMULATED OTHER COMPREHENSIVE LOSS
Description of Capital Stock

The Company is authorized to issue 1,000,000,0001.00 billion shares of common stock, par value $0.01 per share,its Common Stock and 100,000,000100 million shares of preferred stock, par value $0.01 per share. In accordance with the Company'sCompany’s amended and restated certificate of incorporation, each share of common stockCommon Stock has one vote, and the common stockCommon Stock votes together as a single class.
Public Stock Offering
On September 29, 2017, the Company completed a public offering of its common stock (the "Equity Offering"), pursuant to which the Company sold 7.4 million shares, including shares sold pursuant to an exercise of the underwriters' over-allotment option, at a price of $39.10 per share, before underwriting discounts and commissions. Net of these discounts and commissions and other offering expenses, the Company obtained total proceeds from the Equity Offering, including the over-allotment exercise, of $277.8 million. The net proceeds of the Equity Offering, after payment of the discount and related fees and expenses, were used to fund a portion of the consideration for the Catalent Indiana acquisition due at its closing.
Outstanding Stock

Shares outstanding include shares of unvested restricted stock. Unvested restricted stock included in reportable shares outstanding was 0.3 million shares as of December 31, 2017. Shares of unvested restricted stock are excluded from our calculation of basic weighted average shares outstanding, but their dilutive impact is added back in the calculation of diluted weighted average shares outstanding.
Stock Repurchase Program
On October 29, 2015, the Company’s Board of Directors authorized a share repurchase program to use up to $100.0 million to repurchase shares of its outstanding common stock. Under the program, the Company is authorized to repurchase shares through open market purchases, privately negotiated transactions, or otherwise as permitted by applicable federal securities laws. There has been no purchase pursuant to this program as of December 31, 2017.


24



Accumulated Other Comprehensive Income/(Loss)Loss
The components of the changes in the cumulative translation adjustment, derivatives and hedges, minimum pension liability, and available for sale investmentmarketable securities for the three and six months ended December 31, 20172023 and December 31, 20162022 are presented below.
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Table of Contents
 Three Months Ended  
 December 31,
 Six Months Ended  
 December 31,
(Dollars in millions)2017 2016 2017 2016
Foreign currency translation adjustments:       
Net investment hedge$(3.9) $13.6
 $(21.5) $10.0
Long-term intercompany loans(2.3) (13.3) 11.2
 (20.9)
Translation adjustments(5.2) (59.8) 30.9
 (49.2)
Total foreign currency translation adjustment, pretax(11.4) (59.5) 20.6
 (60.1)
Tax expense/(benefit)2.0
 4.9
 (4.1) 3.7
Total foreign currency translation adjustment, net of tax$(13.4) $(64.4) $24.7
 $(63.8)
        
Net change in minimum pension liability       
Net gain/(loss) recognized during the period0.6
 1.0
 1.2
 2.1
Total pension, pretax0.6
 1.0
 1.2
 2.1
Tax expense/(benefit)0.1
 0.3
 0.3
 0.6
Net change in minimum pension liability, net of tax$0.5
 $0.7
 $0.9
 $1.5
        
Net change in available for sale investment:       
Net gain/(loss) recognized during the period(3.6) 24.5
 (8.8) 24.5
Total available for sale investment, pretax(3.6) 24.5
 (8.8) 24.5
Tax expense/(benefit)(0.6) 9.2
 (2.4) 9.2
Net change in available for sale investment, net of tax$(3.0) $15.3
 $(6.4) $15.3
        
Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)2023202220232022
Foreign currency translation adjustments:
Net investment hedge$(38)$(85)$(6)$(4)
Long-term intercompany loans14 31 (2)(10)
Translation adjustments73 155 (5)
Total foreign currency translation adjustment, pretax49 101 — (19)
Tax (benefit) expense12 (17)(2)
Total foreign currency translation adjustment, net of tax$37 $118 $(2)$(17)
Net change in derivatives and hedges:
Net gain recognized during the period$(8)$— $(2)$18 
Total derivatives and hedges, pretax(8)— (2)18 
Tax (benefit) expense(1)— — 
Net change in derivatives and hedges, net of tax$(7)$— $(2)$14 
Net change in minimum pension liability:
Net gain recognized during the period$$— $$— 
Total pension liability, pretax— — 
Tax benefit(1)— (1)— 
Net change in minimum pension liability, net of tax$$— $$— 
Net change in marketable securities:
Net gain recognized during the period$— $$— $
Amounts reclassified from accumulated other
    comprehensive loss
— — 
Net change in marketable securities, pretax— — 
Tax expense— — 
Net change in marketable securities, net of tax$— $$— $
For the three months ended December 31, 2017,2023 and 2022, the changes in accumulated other comprehensive income,loss, net of tax by component are as follows:
(Dollars in millions)Foreign Exchange Translation AdjustmentsPension and Liability AdjustmentsDerivatives and HedgesOtherTotal
Balance at September 30, 2023$(385)$(52)$50 $(1)$(388)
Other comprehensive income (loss) before
    reclassifications
37 — (7)— 30 
Amounts reclassified from accumulated other
    comprehensive loss
— — — 
Net current period other comprehensive
    income (loss)
37 (7)— 34 
Balance at December 31, 2023$(348)$(48)$43 $(1)$(354)
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(Dollars in millions)Foreign Exchange Translation AdjustmentsPension and Liability AdjustmentsDerivatives and HedgesMarketable SecuritiesOtherTotal
Balance at September 30, 2022$(513)$(38)$41 $(3)$(1)$(514)
Other comprehensive income before
    reclassifications
118 — — — — 118 
Amounts reclassified from accumulated other
    comprehensive loss
— — — — 
Net current period other comprehensive
    income
118 — — — 119 
Balance at December 31, 2022$(395)$(38)$41 $(2)$(1)$(395)
For the six months ended December 31, 2023 and 2022, the changes in accumulated other comprehensive loss, net of tax by component are as follows:
(Dollars in millions)Foreign Exchange Translation AdjustmentsPension and Liability AdjustmentsDerivatives and HedgesOtherTotal
Balance at June 30, 2023$(346)$(52)$45 $(1)$(354)
Other comprehensive income (loss) before
    reclassifications
(2)— (2)— (4)
Amounts reclassified from accumulated other
    comprehensive loss
— — — 
Net current period other comprehensive
    income (loss)
(2)(2)— — 
Balance at December 31, 2023$(348)$(48)$43 $(1)$(354)
(Dollars in millions)Foreign Exchange Translation AdjustmentsPension and Liability AdjustmentsDerivatives and HedgesMarketable SecuritiesOtherTotal
Balance at June 30, 2022$(378)$(38)$27 $(4)$(1)$(394)
Other comprehensive (loss) income before
    reclassifications
(17)— 14 — — (3)
Amounts reclassified from accumulated other
    comprehensive loss
— — — — 
Net current period other comprehensive (loss)
    income
(17)— 14 — (1)
Balance at December 31, 2022$(395)$(38)$41 $(2)$(1)$(395)
14.    COMMITMENTS AND CONTINGENCIES
(Dollars in millions)Foreign Exchange Translation Adjustments Pension and Liability Adjustments Available for Sale Investment Adjustments Total
Balance at September 30, 2017$(242.6) $(43.5) $7.1
 $(279.0)
Other comprehensive income/(loss) before reclassifications(13.4) 
 (3.0) (16.4)
Amounts reclassified from accumulated other comprehensive income
 0.5
 
 0.5
Net current period other comprehensive income (loss)(13.4) 0.5
 (3.0) (15.9)
Balance at December 31, 2017$(256.0) $(43.0) $4.1
 $(294.9)

25



For the six months ended December 31, 2017, the changes in accumulated other comprehensive income, net of tax by component are as follows:
(Dollars in millions)Foreign Exchange Translation Adjustments Pension and Liability Adjustments Available for Sale investment Adjustments Total
Balance at June 30, 2017$(280.7) $(43.9) $10.5
 $(314.1)
Other comprehensive income/(loss) before reclassifications24.7
 
 (6.4) 18.3
Amounts reclassified from accumulated other comprehensive income
 0.9
 
 0.9
Net current period other comprehensive income (loss)24.7
 0.9
 (6.4) 19.2
Balance at December 31, 2017$(256.0) $(43.0) $4.1
 $(294.9)

13.
COMMITMENTS AND CONTINGENCIES
The Company continues to receive and resolve claims stemming from a prior, temporary, regulatory suspension of one of our manufacturing facilities. To date, more than 30 customers of the facility have presented claims against the Company for alleged losses, including lost profits and other types of indirect or consequential damages that they have allegedly suffered due to the temporary suspension, or have reserved their right to do so subsequently. The Company is unable to estimate at this time either the total value of claims that are reasonably possible to be asserted with respect to this matter or the likely cost to resolve them, although (a) as of the end of December 31, 2017, the Company has settled 18 customer claims and (b) certain remaining customers have presented the Company with support for other claims having an aggregate claim value of approximately $4.0 million. To date, none of the asserted claims takes into account limitations of liability in the contracts governing these claims or any other defense that the Company may assert. In addition, the Company may have insurance for additional costs it may incur as a result of such claims, subject to various deductibles and other limitations, but there can be no assurance as to the aggregate amount or timing of insurance recoveries against any such costs.Litigation
From time to time, the Company may be involved in legal proceedings arising in the ordinary course of business, including, without limitation, inquiries and claims concerning environmental contamination as well as litigation and allegations in connection with acquisitions, product liability, manufacturing or packaging defects, and claims for reimbursement for the cost of lost or damaged active pharmaceutical ingredients, the cost of any of which could be significant. Such matters are inherently uncertain, and there can be no guarantee that the outcome of any such matter will be decided favorably to the Company or that the resolution of any such matter will not have a material adverse effect upon the Company’s consolidated financial statements. The Company records a liability in its consolidated financial statements for these matters when a loss is known or considered probable and the amount can be reasonably estimated. The Company reviews these estimates each accounting period as additional information is known and adjusts the loss provision when appropriate. If a matter is both probable to result in a liability and the amount of loss can be reasonably estimated, the Company estimates and discloses the
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possible loss or range of loss to the extent necessary for its consolidated financial statements not to be misleading. If the loss is not probable or cannot be reasonably estimated, a liability is not recorded in the Company's consolidated financial statements. Any legal or other expenses associated with the litigation are accrued for as the expenses are incurred. The Company intends to vigorously defend itself against any such litigation and does not currently believe that the outcome of any such litigation will have a material adverse effect on the Company’s consolidated financial statements. In addition, the healthcare industry is highly regulated and government agencies continue to scrutinize certain practices affecting government programs and otherwise.

City of Warwick Retirement System Class Action

In February 2023, an alleged shareholder filed a complaint styled City of Warwick Retirement System v. Catalent, Inc., et al., No. 23-cv-01108, in New Jersey federal court against the Company and three of its then-officers (collectively, “the Warwick Defendants”) purportedly on behalf of a putative “class” consisting of persons who purchased or otherwise acquired Company securities between August 30, 2021 and October 31, 2022, inclusive. On September 15, 2023, the Warwick complaint was amended (together with the original complaint, the "Warwick Complaint"), which amended complaint expanded the class period to between August 30, 2021 and May 7, 2023, inclusive (the “Class Period”). The Warwick Complaint purports to assert claims under Section 10(b) and 20(a) of the Securities Exchange Act of 1934, as amended and the related regulations, alleging that, unbeknownst to investors, the Warwick Defendants purportedly engaged in accounting and channel stuffing schemes to pad the Company’s revenues and failed to disclose adverse facts that purportedly were known to or recklessly disregarded by the Warwick Defendants. Specifically, the Warwick Complaint alleges that the Warwick Defendants (i) overstated revenue and earnings by prematurely recognizing revenue in violation of U.S. GAAP; (ii) suffered material weaknesses in its internal controls over financial reporting related to revenue recognition; (iii) falsely represented demand for its products while knowingly selling more product to its direct customers than could be sold to healthcare providers and end consumers; (iv) cut corners on safety and control procedures at key production facilities; (v) disregarded regulatory rules at key production facilities in order to rapidly produce excess inventory that was used to pad the Company’s financial results through premature revenue recognition in violation of U.S. GAAP or stuffing its direct customers with this excess inventory; and (vi) lacked a reasonable basis for their positive statements about the Company’s financial performance, outlook, and regulatory compliance during the Class Period. The Company believes that the Warwick Defendants have defenses to the allegations and claims set forth in the complaint and filed a motion to dismiss the Warwick Complaint on November 15, 2023. The plaintiffs filed their opposition to the Company's motion to dismiss on January 12, 2024, and the Company's reply to the plaintiffs' opposition is due February 15, 2024.

Husty Derivative Claim

In August 2023, an alleged shareholder filed a derivative complaint styled Husty et al. v. Carroll, et al., No. 23-cv-00891, in Delaware federal court against certain current and former members of the Company's board of directors, (the Husty Defendants), and nominally against Catalent, Inc. The complaint mimics the allegations set out in the original complaint filed in the City of Warwick Retirement System action described aboveand claims that the alleged activities described there led to, and will continue to expose the Company to, costs and damages. The Company believes that the Husty Defendants have defenses to the allegations and claims set forth in the complaint and, once all Husty Defendants are properly served with the complaint, intends to vigorously defend the Husty Defendants against such allegations.

Brown Derivative Claim

In September 2023, an alleged shareholder filed a derivative complaint styled Brown, et al. v. Chiminski, et al., Case 3:23-cv-15722, in New Jersey federal court against certain current and former officers and members of the Company's board of directors (the Brown Defendants) and nominally against Catalent, Inc. The complaint mimics the allegations set out in the original complaint filed in the City of Warwick Retirement System action described above and claims that the alleged activities described there led to, and will continue to expose the Company to, costs and damages. On November 8, 2023, the court entered a stipulation between the parties extending the Brown Defendants’ time to respond to the complaint until January 19, 2024. The Company believes that the Brown Defendants have defenses to the allegations and claims set forth in the complaint and intends to vigorously defend the Brown Defendants against such allegations.

Subpoenas and Requests for Information

From time to time, the Company receives subpoenas or requests for information relating to the business practices and activities of customers or suppliers from various governmental agencies or private parties, including from state attorneys general, the U.S. Department of Justice, and private parties engaged in patent infringement, antitrust, tort, and other litigation.parties. The Company generally responds to such subpoenas and requests in a timely and thorough manner, which responses sometimes require considerable time and effort and can result in considerable costs being incurred.

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In June 2023, the Company received a demand from a company stockholder pursuant to 8 Del. C. § 220 to inspect books and records of the Company relating to, among other things, the allegations raised in the Warwick Complaint. The Company expectshas responded to incur coststhe demand and cannot determine at this time if the books and records demand will lead to litigation.

Fire at Biologics Facility

During the three months ended December 31, 2023, the Company had a small fire at a facility in future periodsits Biologics segment. The fire activated the sprinkler systems, which then caused minor flooding in connection with future requests.
14.SEGMENT INFORMATION
certain parts of the facility. The Company conducts its business withinaccrued $9 million for estimated damages, repairs, and lost inventory. The Company is insured for such incidents and has submitted claims for reimbursement. Proceeds from potential reimbursement are not included in the following operating segments: Softgel Technologies, Drug Delivery Solutions,financial statements for the three and Clinical Supply Services. six months ended December 31, 2023.
15.    SEGMENT INFORMATION
The Company evaluates the performance of its segments based on segment earnings before noncontrolling interest, other (income) expense,(expense) income, impairments, restructuring costs, interest expense, income tax (benefit)/expense, and depreciation and amortization (“Segment EBITDA”).
Segment EBITDA from continuing operations is subject to important limitations. These consolidated earnings from continuing operations before interest expense, income tax (benefit)/expense, depreciationfinancial statements include information concerning Segment EBITDA (a) because Segment EBITDA is an operational measure used by management in the assessment of the operating segments, the allocation of resources to the segments, and amortizationthe setting of strategic goals and is adjustedannual goals for the income or loss attributablesegments, and (b) in order to noncontrolling interest.provide supplemental information that the Company considers relevant for the readers of the consolidated financial statements. The Company’s presentation of Segment EBITDA and EBITDA from continuing operations are not defined in GAAP and may not be comparable to similarly titled measures used by other companies.

26



The following tables include net revenue and Segment EBITDA for each of the Company's current reportable segments during the three and six months ended December 31, 20172023 and December 31, 2016:
2022:
 Three Months Ended  
 December 31,
 Six Months Ended  
 December 31,
(Dollars in millions)2017 2016 2017 2016
Softgel Technologies       
Net revenue$228.1
 $201.9
 $447.8
 $388.3
Segment EBITDA50.1
 43.4
 85.2
 73.9
Drug Delivery Solutions       
Net revenue285.4
 214.0
 511.2
 405.3
Segment EBITDA81.1
 50.0
 128.5
 92.0
Clinical Supply Services       
Net revenue108.7
 77.0
 218.4
 152.0
Segment EBITDA19.0
 11.6
 35.7
 22.1
Inter-segment revenue elimination(15.9) (9.2) (27.2) (19.7)
Unallocated Costs (1)
(48.2) (19.8) (82.2) (40.1)
Combined Totals:       
Net revenue$606.3
 $483.7
 $1,150.2
 $925.9
        
EBITDA from continuing operations$102.0
 $85.2
 $167.2
 $147.9
(Dollars in millions)Three Months Ended  
December 31,
Six Months Ended  
December 31,
2023202220232022
Segment EBITDA reconciled to net (loss) earnings:
Biologics$38 $181 $87 $294 
Pharma and Consumer Health126 135 227 243 
Sub-Total$164 $316 $314 $537 
Reconciling items to net earnings
Unallocated costs (1)
(159)(52)(936)(139)
Depreciation and amortization(121)(103)(233)(202)
Interest expense, net(66)(47)(124)(79)
Income tax (expense) benefit(24)(33)14 (36)
Net (loss) earnings$(206)$81 $(965)$81 

(1)Unallocated costs include restructuring and special items, equity-based(1) Unallocated costs include restructuring and special items, stock-based compensation, impairment charges, certain other corporate directed costs, and other costs that are not allocated to the segments as follows:
 Three Months Ended  
 December 31,
 Six Months Ended  
 December 31,
(Dollars in millions)2017 2016 2017 2016
Impairment charges and gain/(loss) on sale of assets$(4.2) $(0.5) $(4.2) $(0.5)
Equity compensation(8.5) (4.9) (15.5) (11.8)
Restructuring and other special items (2)
(11.9) (7.2) (24.2) (13.1)
Other income/(expense), net (3)
(13.6) 1.8
 (19.3) 3.9
Non-allocated corporate costs, net(10.0) (9.0) (19.0) (18.6)
Total unallocated costs$(48.2) $(19.8) $(82.2) $(40.1)
(2)Segment results do not include restructuring and certain acquisition-related costs.
(3)Refer to Note 7 for details of financing charges and foreign currency translation adjustments recorded within other income/(expense), net.
Provided below is a reconciliation of EBITDA from continuing operations to earnings/(loss) from continuing operations:
 Three Months Ended  
 December 31,
 Six Months Ended  
 December 31,
(Dollars in millions)2017 2016 2017 2016
Earnings/(loss) from continuing operations$(21.9) $17.4
 $(18.1) $22.0
Depreciation and amortization46.8
 35.5
 85.8
 71.3
Interest expense, net27.2
 22.8
 51.5
 44.9
Income tax expense/(benefit)49.9
 9.5
 48.0
 9.7
EBITDA from continuing operations$102.0
 $85.2
 $167.2
 $147.9

the segments as follows:                                                        
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(Dollars in millions)Three Months Ended  
December 31,
Six Months Ended  
December 31,
2023202220232022
Impairment charges and gain/loss on sale of assets(a)
$(15)$(1)$(14)$
Stock-based compensation(16)(10)(35)(29)
Restructuring and other special items(b)
(83)(33)(106)(42)
Goodwill impairment adjustments (charges)(c)
— (687)— 
Pension settlement charges(3)— (3)— 
Other (expense) income, net(d)
(4)23 (17)(2)
Unallocated corporate costs, net(40)(31)(74)(67)
Total unallocated costs$(159)$(52)$(936)$(139)

(a)    Impairment charges and gain/loss on sale of assets for the three and six months ended December 31, 2023 includes fixed asset impairment charges associated with equipment for a product with significant decline demand in the Company's Biologics segment.
(b)    Restructuring and other special items during the three months ended December 31, 2023 include (i) restructuring charges associated with plans to reduce costs, consolidate facilities, and optimize our infrastructure across the organization and (ii) transaction and integration costs associated with the Metrics acquisition. For further details on restructuring charges, see Note 8, Restructuring Costs to the Consolidated Financial Statements.
Restructuring and other special items during the three months ended December 31, 2022 include (i) restructuring charges associated with our plans to reduce costs, consolidate facilities, and optimize our infrastructure across the organization and (ii) transaction and integration costs associated with our Metrics acquisition. Restructuring and other special items for the six months ended December 31, 2022 also includes warehouse exit costs for a product the Company no longer manufactures in its Pharma and Consumer Health segment. For further details on restructuring charges, see Note 8, Restructuring Costs to the Consolidated Financial Statements.
(c)    Goodwill impairment charges during the six months ended December 31, 2023 were associated with the Company's Consumer Health and Biomodalities reporting units, which are part of the Company's Pharma and Consumer Health and Biologics segments, respectively. For further details, see Note 4, Goodwill to the Consolidated Financial Statements.
(d)    Other expense, net during the three months ended December 31, 2023 and 2022 primarily includes foreign currency remeasurement losses/gains.

The following table includes total assets for each segment, as well as reconciling items necessary to total the amounts reported in the consolidated financial statements:statements.
(Dollars in millions)December 31,
2023
June 30,
2023
Assets:
Biologics$5,363 $5,746 
Pharma and Consumer Health4,517 4,867 
Corporate and eliminations108 164 
Total assets$9,988 $10,777 
32
(Dollars in millions)December 31, 
 2017
 June 30, 
 2017
Assets   
Softgel Technologies$1,538.4
 $1,631.8
Drug Delivery Solutions2,650.5
 1,639.0
Clinical Supply Services620.3
 596.2
Corporate and eliminations(422.1) (412.7)
Total assets$4,387.1
 $3,454.3

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16. SUPPLEMENTAL BALANCE SHEET INFORMATION
15.SUPPLEMENTAL BALANCE SHEET INFORMATION
SupplementarySupplemental balance sheet information at December 31, 20172023 and June 30, 20172023 is detailed in the following tables.
Inventories
Work-in-process and finished goods inventories include raw materials, labor, and overhead. Total inventories consist of the following:
(Dollars in millions)December 31, 
 2017
 June 30, 
 2017
(Dollars in millions)December 31,
2023
June 30,
2023
Raw materials and supplies$134.3
 $107.5
Work-in-process29.3
 42.8
Finished goods69.9
 56.7
Total inventories, gross
Total inventories, gross
Total inventories, gross233.5
 207.0
Inventory cost adjustment(20.8) (22.1)
Inventories$212.7
 $184.9
Total inventories
Prepaid expenses and other
Prepaid expenses and other current assets consist of the following:
(Dollars in millions)December 31, 
 2017
 June 30, 
 2017
Prepaid expenses$19.0
 $12.3
Spare parts supplies11.4
 11.8
Prepaid income tax10.5
 11.5
Non-US value added tax19.9
 16.0
Available for sale investment9.8
 18.6
Other current assets34.8
 27.6
Prepaid expenses and other$105.4
 $97.8

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Property, plant, and equipment, net
Property, plant, and equipment, net consist of the following:
(Dollars in millions)December 31, 
 2017
 June 30, 
 2017
Land, buildings, and improvements$894.2
 $735.2
Machinery, equipment, and capitalized software944.1
 825.0
Furniture and fixtures13.5
 10.1
Construction in progress179.9
 137.4
Property, plant, and equipment, at cost2,031.7
 1,707.7
Accumulated depreciation(775.5) (711.8)
Property, plant, and equipment, net$1,256.2
 $995.9
(Dollars in millions)December 31,
2023
June 30,
2023
Prepaid expenses$58 $53 
Short-term contract assets478 399 
Spare parts supplies27 24 
Prepaid income tax75 77 
Non-U.S. value-added tax45 38 
Other current assets40 42 
Total prepaid expenses and other$723 $633 
Other accrued liabilities
Other accrued liabilities consist of the following:
(Dollars in millions)December 31,
2023
June 30,
2023
Contract liabilities$214 $167 
Accrued employee-related expenses136 160 
Accrued expenses141 134 
Operating lease liabilities11 
Restructuring accrual16 19 
Accrued interest39 35 
Accrued income tax28 44 
Total other accrued liabilities$583 $570 
Allowance for credit losses
The rollforward of allowance for credit losses for the six months ended December 31, 2023 is as follows:
Allowance for credit losses
(Dollars in millions)
Balance, June 30, 2023$46 
Charges (Credits)(4)
Balance, December 31, 2023$42 

33
(Dollars in millions)December 31, 
 2017
 June 30, 
 2017
Accrued employee-related expenses$72.6
 $96.4
Restructuring accrual3.0
 5.9
Accrued interest5.6
 0.9
Deferred revenue and fees88.1
 84.9
Accrued income tax22.2
 24.7
Other accrued liabilities and expenses58.3
 68.4
Other accrued liabilities$249.8
 $281.2


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17.     SUBSEQUENT EVENTS
Entry Into an Agreement and Plan of Merger
On February 5, 2024, the Company entered into the Agreement and Plan of Merger (the “Merger Agreement”), with Creek Parent, Inc. (“Parent”), a Delaware corporation and a wholly owned subsidiary of Novo Holdings A/S (“Novo Holdings”), and Creek Merger Sub, Inc., a Delaware corporation and a wholly owned subsidiary of Parent (“Merger Sub”). The Merger Agreement provides that, upon the terms and subject to the conditions set forth therein and in accordance with the General Corporation Law of the State of Delaware (the “DGCL”), Merger Sub will be merged with and into the Company (the “Merger”), with the Company surviving the Merger as a wholly owned subsidiary of Parent. Parent will acquire all the issued and outstanding shares of common stock of the Company.

At the effective time of the Merger (the “Effective Time”), each share of common stock, par value $0.01 per share, of the Company (such shares, collectively, the “Company Common Stock,” and each, a “Share”) that is issued and outstanding immediately prior to the Effective Time (other than any Shares held by (i) the Company, Parent or Merger Sub or any other direct or indirect wholly owned subsidiary of the Company or Parent immediately prior to the Effective Time, or (ii) a holder who has not voted in favor of the adoption of the Merger Agreement and is entitled to demand and properly demands appraisal of such Shares under the DGCL), will be converted automatically into the right to receive an amount in cash equal to $63.50 per Share, without interest (the “Merger Consideration”). The transaction values the Company at $16.5 billion on an enterprise value basis.

Consummation of the Merger is subject to customary closing conditions, including approval of the Merger by the Company’s stockholders (which has not been obtained at this stage). Further conditions include (i) receipt of certain governmental waivers, consents, clearances, decisions, declarations, approvals, and expirations of applicable waiting periods, including the expiration or early termination of the waiting period under the U.S. Hart-Scott-Rodino Antitrust Improvements Act of 1976, with respect to (A) the Merger and (B) the sale of three of the Company’s fill-finish sites (which are located in Anagni, Italy, Bloomington, Indiana USA, and Brussels, Belgium) and related assets from Novo Holdings to Novo Nordisk A/S (“Novo Nordisk”), of which Novo Holdings is the controlling shareholder (the “Carve-Out”), and (ii) the absence of any order, injunction or law prohibiting the Merger or the Carve-Out, in each case, without a Burdensome Condition (as defined in the Merger Agreement). Parent’s and Merger Sub’s obligations to close the Merger are also conditioned upon the absence of a Material Adverse Effect (as defined in the Merger Agreement) on the Company.

Upon termination of the Merger Agreement with Parent, the Company, under specified circumstances and conditions set forth in the Merger Agreement, could be required to pay Parent a termination fee of approximately $345 million.
ITEM 2.
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

The Company
We are the leading global provider of advanced delivery technologiesprovide differentiated development and developmentmanufacturing solutions for drugs, protein-based biologics, cell and gene therapies, vaccines, and consumer health products at over fifty facilities across four continents under rigorous quality and animal health products.operational standards. Our oral, injectable, and respiratory delivery technologies, provide delivery solutionsalong with our state-of-the-art protein, plasmid, viral, and cell and gene therapy manufacturing capacity, address a wide and growing range of modalities and therapeutic and other categories across the full diversity of thebiopharmaceutical, pharmaceutical, industry, including small molecules, biologics, and consumer and animal health products.industries. Through our extensive capabilities, growth-enabling capacity, and deep expertise in product development, regulatory compliance, and clinical trial and commercial supply, we can help our customers take products to market faster, including nearlymore than half of new drug products approved by the FDAU.S. Food and Drug Administration (the “FDA”) in the last decade. Our advanced delivery technologydevelopment and manufacturing platforms, which include those in our Softgel Technologies and our Drug Delivery Solutions segments, our proven
formulation, manufacturingsupply, and regulatory expertise, and our broad and deep intellectual propertydevelopment and manufacturing know-how enable our customers to advance and their patients' needsthen bring to developmarket more products and better treatments for patients and consumers. Across both development and delivery, ourOur commitment to reliably supply our customers’ and their patients’ needs is the foundation for the value we provide; annually, we produce approximately 7270 billion unit doses for nearly 7,0008,000 customer prescription and consumer health products, or approximately one1 in every twenty26 unit doses of such products taken each year by patients and consumers around the world. We believe that, through our investments in growth-enablingstate-of-the-art facilities and capacity expansion, including investments in facilities focused on new treatment modalities and capabilities,other attractive market segments, our ongoing focus oncontinuous improvement activities devoted to operational and quality excellence, the sales of existing customer products, theand introduction of new customer products, and, in some cases, our innovation activities and patents, and our entry into new markets, we will continue to benefit from attractive and differentiated margins,attract premium opportunities and realize the growth potential from these areas.

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Our operating structure consists of two operating and reportable segments: (i) Biologics, and (ii) Pharma and Consumer Health. The Biologics segment provides formulation, development, and manufacturing for biologic proteins, cell gene, and other nucleic acid therapies; pDNA; iPSCs, oncolytic viruses, and vaccines; formulation, development, and manufacturing for parenteral dose forms, including vials, prefilled syringes, and cartridges; and analytical development and testing services for large molecules. Our Pharma and Consumer Health segment provides market-leading capabilities for complex oral solids, softgel formulations, Zydis fast-dissolve technologies, and gummy, soft chew, and lozenge dosage forms; formulation, development, and manufacturing platforms for oral, nasal, inhaled, and topical dose forms; cold-chain storage and distribution, and clinical trial development and supply services.

Critical Accounting Policies and Estimates
We prepare our financial statements in accordance with GAAP. These standards require management to makegenerally accepted accounting principles in the United States (“U.S. GAAP”). Management made certain estimates and assumptions thatduring the preparation of the Consolidated Financial Statements in accordance with U.S. GAAP. These estimates and assumptions affect amountsthe reported amount of assets and liabilities and disclosures of contingent assets and liabilities in the consolidated financial statementsstatements. These estimates also affect the reported amount of net earnings during the reporting periods. Actual results could differ from those estimates. Because of the size of the financial statement elements to which they relate, some of our accounting policies and accompanying notes. Such estimates include, buthave a more significant impact on the Consolidated Financial Statements than others.
Goodwill and Indefinite-Lived Intangible Assets
We account for purchased goodwill and intangible assets with indefinite lives in accordance with ASC 350, Intangibles – Goodwill and Other. Under ASC 350, goodwill and intangible assets with indefinite lives are not limitedamortized, but instead are tested for impairment at least annually. We perform an impairment evaluation of goodwill annually during the fourth quarter of our fiscal year or when circumstances otherwise indicate an evaluation should be performed. The evaluation may begin with a qualitative assessment for each reporting unit to allowancedetermine whether it is more likely than not that the fair value of the reporting unit is less than its carrying value. If the qualitative assessment does not generate a positive response, or if no qualitative assessment is performed, a quantitative assessment, based upon discounted cash flows, is performed and requires management to estimate future cash flows, growth rates, and economic and market conditions.
As a result of Consumer Health's underperformance of recent operating results relative to expectations, as well as current macroeconomic conditions impacting the consumer health and biotechnology industries, and higher interest rates, we assessed the current and future economic outlook as of September 30, 2023 for doubtful accounts, inventoryour Consumer Health and long-lived asset valuation,Biomodalities reporting units in our Pharma and Consumer Health and Biologics segments, respectively, and identified indicators for impairment of goodwill.
The evaluation began with a qualitative assessment of each reporting unit to determine if it was more likely than not that the fair value of the reporting unit was less than its carrying value. The qualitative assessment did not indicate that it was more likely than not that the fair value exceeded the carrying value in our Consumer Health and Biomodalities reporting units, which led to a quantitative assessment for the corresponding reporting units. The evaluation performed as of September 30, 2023 resulted in a combined goodwill impairment charge of $689 million for our Consumer Health and other intangible assetBiomodalities reporting units within the Pharma and Consumer Health and Biologics segments, respectively.
A 50 basis point increase in the discount rate would increase the goodwill impairment income taxes, derivative financial instruments, self-insurance accruals, loss contingencies$220 million and restructuring charge reserves. Actual amounts may differ from these estimated amounts.$50 million for its Biomodalities and Consumer Health reporting units, respectively. A 50 basis point decrease in the long-term growth rate would increase the goodwill impairment by $120 million and $30 million for its Biomodalities and Consumer Health reporting units, respectively.
ThereFor further details on the impairment charges for the six months ended December 31, 2023, see Note 4, Goodwill to our Consolidated Financial Statements.
Other than the above, there was no material change to our critical accounting policies or in the underlying accounting assumptions and estimates from those described in our fiscal year 2017 Annual Report on Form 10-K, other than recently adopted accounting principles as disclosed in Note 1 to the unaudited consolidated financial statements included elsewhere in this Quarterly Report on Form 10-Q, which adoption had no material impact on net earnings.Fiscal 2023 10-K.
Non-GAAP Performance Metrics
Use of EBITDA from continuing operations
Management measures operating performance based on consolidated earnings from continuing operations before interest expense, expense/(benefit)expense for income taxes, and depreciation and amortization, (“adjusted for the income or loss attributable to non-controlling interests (EBITDA from continuing operations”). EBITDA from continuing operations is not defined under U.S. GAAP, and is not a measure of
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operating income, operating performance, or liquidity presented in accordance with U.S. GAAP, and is subject to important limitations.
We believe that the presentation of EBITDA from continuing operations enhances an investor’s understanding of our financial performance. We believe this measure is a useful financial metric to assess our operating performance from period to period by excluding certain items that we believe are not representative of our core business and use this measure for business planning purposes. In addition, given the significant historical investments that we have made in the past in property, plant, and equipment, depreciation and amortization expenses represent a meaningful portion of our cost structure. We believe that EBITDA from continuing operations will provide investors with a useful tool for assessing the comparability between periods of our ability to generate cash from operations sufficient to pay taxes, to service debt, and to undertake capital expenditures because it eliminates depreciation and amortization expense. We present EBITDA from continuing operations in order to provide supplemental information that we consider relevant for the readers of our consolidated financial statements,the Consolidated Financial Statements, and such information is not meant to replace or supersede U.S. GAAP measures. Our definition of EBITDA from continuing operations may not be the same as similarly titled measures used by other companies. The most directly comparable GAAP measure to EBITDA from continuing operations defined under U.S. GAAP is earnings/(loss) from continuing operations.net earnings. Included in this reportManagement’s Discussion and Analysis is a reconciliation of earnings/(loss) from continuing operationsnet earnings to EBITDA from continuing operations.

In addition, we evaluate the performance of our segments based on segment earnings before noncontrolling interest,non-controlling interests, other expense (income)/expense,, impairments, restructuring costs, interest expense, income tax expense/(benefit),expense, and depreciation and amortization (“(Segment EBITDA”).

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Segment EBITDA to net earnings, see Note 15, Segment Information to our Consolidated Financial Statements.
Use of Constant Currency
As exchange rates are an important factor in understanding period-to-period comparisons, we believe the presentation of results on a constant currencyconstant-currency basis in addition to reported results helps improve investors’ ability to understand our operating results and evaluate our performance in comparison to prior periods. Constant currencyConstant-currency information compares results between periods as if exchange rates had remained constant period-over-period. We use results on a constant currencyconstant-currency basis as one measure to evaluate our performance. In this Quarterly Report on Form 10-Q, we compute constant currency by calculating current-yearcurrent period results using prior-yearprior period foreign currency exchange rates. We generally refer to such amounts calculated on a constant currencyconstant-currency basis as excluding the impact of foreign currency exchange. These results should be considered in addition to, not as a substitute for, results reported in accordance with U.S. GAAP. Results on a constant currencyconstant-currency basis, as we present them, may not be comparable to similarly titled measures used by other companies and are not measures of performance presented in accordance with U.S. GAAP.
Other Non-GAAP Measures
Organic revenue growth and segmentSegment EBITDA growth are useful measures calculated by the Companywe use to explain the underlying results and trends in the business. Organic revenue growth and segmentSegment EBITDA growth are measures used to show current yearperiod sales and earningsprofitability from existing operations and include joint ventures and revenue from product participation related activities entered into within the year.operations. Organic revenue growth and segmentSegment EBITDA growth exclude the impact of foreign currency exchange, acquisitions of operating or legal entities, and divestitures within the year.applicable periods. These measures should be considered in addition to, not as a substitute for, performance measures reported in accordance with U.S. GAAP. These measures, as we present them, may not be comparable to similarly titled measures used by other companies and are not measures of performance presented in accordance with U.S. GAAP.
Three Months Ended December 31, 20172023 Compared to the Three Months Ended December 31, 20162022
ResultsThe below tables summarize several financial metrics we use to measure performance for the three months ended December 31, 2017 compared2023 and 2022. Refer to the discussions below regarding performance and use of key financial metrics.
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4606MDA Chart Graph Q2 QTD v9.jpg

Results for the three months ended December 31, 20162023 compared to the three months ended December 31, 2022 were as follows:
 Three Months Ended  
 December 31,
 FX impact Constant Currency Increase/(Decrease)
(Dollars in millions)2017 2016 
 Change $ Change %
Net revenue$606.3
 $483.7
 $17.0
 $105.6
 22 %
Cost of sales418.9
 335.8
 12.7
 70.4
 21 %
Gross margin187.4
 147.9
 4.3
 35.2
 24 %
Selling, general and administrative expenses114.3
 96.2
 1.1
 17.0
 18 %
Impairment charges and (gain)/loss on sale of assets4.2
 0.5
 0.1
 3.6
 *
Restructuring and other0.1
 3.3
 
 (3.2) (97)%
Operating earnings68.8
 47.9
 3.1
 17.8
 37 %
Interest expense, net27.2
 22.8
 0.3
 4.1
 18 %
Other (income)/expense, net13.6
 (1.8) 1.4
 14.0
 *
Earnings from continuing operations, before income taxes28.0
 26.9
 1.4
 (0.3) (1)%
Income tax expense/(benefit)49.9
 9.5
 
 40.4
 *
Net earnings/(loss)$(21.9) $17.4
 $1.4
 $(40.7) *
 Three Months Ended  
December 31,
FX ImpactConstant Currency Increase (Decrease)
(Dollars in millions)20232022Change $Change %
Net revenue$1,024 $1,149 $15 $(140)(12)%
Cost of sales853 762 12 79 10 %
Gross margin171 387 (219)(56)%
Selling, general, and administrative expenses250 226 22 10 %
Goodwill impairment adjustments(2)— — (2)*
Other operating expense, net35 23 11 39 %
Operating (loss) earnings(112)138 — (250)*
Interest expense, net66 47 18 39 %
Other expense (income), net(23)(1)28 *
(Loss) earnings before income taxes(182)114 — (296)*
Income tax expense24 33 — (9)(28)%
Net (loss) earnings$(206)$81 $— $(287)*
 *Percentage not* Not meaningful
Change % calculations are based on amounts prior to rounding
Net Revenue
2023 vs. 2022
Year-Over-Year ChangeThree Months Ended  
December 31,
Net Revenue
Organic(12)%
Constant-currency change(12)%
Foreign currency translation impact on reporting%
Total % change(11)%

Net revenue increased $105.6decreased $140 million, or 22%12%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2022. Net revenue decreased 12% organically primarily due to a decline in demand for COVID-19 related programs, and a decline in demand for our consumer health products, primarily our wellness products, partially offset by
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growth from the manufacture of prescription products, gene therapy offerings, and our orally delivered Zydis commercial products.
Gross Margin

Gross margin decreased $219 million, or 56%, compared to the three months ended December 31, 2016,2022, excluding the impact of foreign exchange. Net revenue increased 14% as a result of acquisitions. We acquired Cook Pharmica LLC (now doing business as Catalent Indiana, LLC, "Catalent Indiana") in October 2017, which is included within our Drug Delivery Solutions segment and Accucaps Industries Limited ("Accucaps") in February 2017, which is in our Softgel Technologies segment. Excluding the impact of acquisitions, net revenue increased by 8%, primarily due to increased volume in lower-margin comparator sourcing volume and our storage and distribution business within our Clinical Supply Services segment, timing of a standard maintenance shut-down at our European sterile pre-filled syringe facility and increased volume within our biologics offerings within our Drug Delivery Solutions segment.

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Gross Margin
Gross margin increased $35.2 million, or 24%, compared to the three months ended December 31, 2016, excluding the impact of foreign exchange. Gross margin increased across all three reportable segments primarily due to increased sales volumes as discussed above. On a constant-currency basis, gross margin, as a percentage of revenue, increased 50decreased 1,680 basis points to 31.1%16.7% in the three months ended December 31, 2017,2023, compared to 30.6%33.5% in the prior year period. The increase wasprior-year period, primarily due to a favorablean unfavorable shift in product mix, shift to certain higher margin offerings within our oral delivery solutionslower levels of utilization across the network, increased spending on operational and biologics offeringsengineering enhancements in our U.S. operations within our Drug Delivery SolutionsBiologics segment, partially offset by a decreasean increase in our product participation revenue within both our Softgel Technologies segmentinventory write-offs and our Drug Delivery Solutions segment.reduced productivity.
Selling, General, and Administrative Expenses

Selling, general, and administrative expenses increased $17.0$22 million, or 18%10%, compared to the three months ended December 31, 2016,2022, excluding the impact of foreign exchange. The year-over-year increase was attributable to higher costs due to increased spending on operational and engineering enhancements, and a $6 million increase in stock-based compensation, which were partially offset by a $7 million benefit from a decline in credit losses.
Other Operating Expense, net
Other operating expense, net for the three months ended December 31, 2023 increased $11 million or 39%, excluding the impact of foreign exchange, primarily duecompared to additional expenses from recently acquired companies of $9 million, which includes $5 million of incremental depreciation and amortization expense and $2 million of employee related costs. Additionally, the three months ended December 31, 2017 includes one-time transaction fees of $2 million related to the acquisition of Catalent Indiana in October 2017. Selling, general and administrative expenses further increased approximately $4 million for non-cash equity based compensation2022. This increase was primarily driven by higher expense for certain performance based awardsa $14 million increase in the current period.
Impairmentfixed asset impairment charges and (gain)/loss on sale$3 million of assetspension settlement charges.
Impairment charges and loss on saleInterest Expense, net
Interest expense, net of assets of $4.2 million includes the loss on sale of two Softgel Technologies segment manufacturing sites in the Asia Pacific region. The site divestitures were neither material individually or in aggregate to the segment or to the Company.
Restructuring and Other
Restructuring and other costs of $0.1$66 million for the three months ended December 31, 2017 decreased $3.2 million compared to the three months ended December 31, 2016. Other costs in the three months ended December 31, 2016, included claim resolution charges of $3.2 million (without regard to possible future insurance recoveries), related to a previous temporary regulatory suspension at one of our manufacturing facilities. Restructuring expense will vary period to period based on the level of acquisitions during the year and site consolidation efforts to further streamline the business.
Interest Expense, net
Interest expense, net of $27.2 million for the three months ended December 31, 20172023 increased by $4.4$18 million, or 19%39%, compared to the three months ended December 31, 2016,2022, excluding the impact of foreign exchange. The increase was primarily driven by an averageattributable to higher level of outstanding debt associated with the financing for the Catalent Indiana acquisition in October 2017, partially offset by principal payments on our term loans and an overall reduction in our interest rates on our senior secured credit facility compared tovariable rate debt and incremental borrowings.

For additional information concerning our debt and financing arrangements, including the prior-year period.
On October 18, 2017, we completed a private offering (the "Debt Offering")changing mix of $450 million aggregate principal amount of 4.875% senior unsecured notes due 2026 (the "USD Notes"). The USD Notes will mature on January 15, 2026, bear interest at the rate of 4.875% per annum,debt and are payable semi-annuallyequity in arrears on January 15our capital structure, see “—Liquidity and July 15 of each year beginning on July 15, 2018. The net proceeds of the Debt Offering, after payment of the initial purchasers' discountCapital Resources” below and related feesNote 5, Long-Term Obligations and expenses, were used to fund a portion of the Catalent Indiana acquisition consideration at its closing.
Concurrent with the Debt Offering, we completed the Third Amendment (the "Third Amendment")Short-Term Borrowings to our Amended and Restated Credit Agreement (as amended, the "Credit Agreement"), which lowered the interest rate on U.S. dollar-denominated and euro-denominated term loans and the revolving credit facility and extended the maturity dates on the senior secured credit facilities by three years. The new applicable rate for U.S. dollar-denominated term loans decreased 0.50%, and the new applicable rate for euro-denominated term loans is LIBOR decreased 0.75%. The new applicable rate for the revolving loans decreased 1.25%.
Further, a component of the purchase price for the Catalent Indiana acquisition consists of $200 million in deferred purchase consideration payable in $50 million installments, on each anniversary of the closing date over a period of four years, which is accounted for as debt and includes a component of imputed interest expense.
On December 9, 2016, we completed a private offering of €380.0 million aggregate principal of 4.75% Senior Notes due 2024 (the "Euro Notes"). The Euro Notes will mature on December 15, 2024, bear interest at the rate of 4.75% per annum and are payable semi-annually in arrears on June 15 and December 15 of each year.

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Consolidated Financial Statements.
Other (Income)/Expense, net
Other expense, was $13.6net of $4 million for the three months ended December 31, 2017, compared to $1.82023 was primarily driven by $4 million of otherforeign currency losses.

Other income, net of $23 million for the three months ended December 31, 2016. The expense in the three months ended December 31, 20172022 was primarily driven by $11.8$25 million of financing charges related to the USD Notes offering and the Third Amendment, and includes a $6.1 million charge for commitment fees paid during the first quarter of fiscal 2018 on a proposed bridge loan made available to us for the purpose of providing back-up financing to fund a portion of the Catalent Indiana acquisition purchase price (the "Bridge Facility").
The three months ended December 31, 2016 of $1.8 million was primarily driven by non-cash net gains of $5.3 million related to foreign currency translation, partially offset by $4.3 million of financing charges related to the December 2016 private offering of the Euro Notes and repricing and partial paydown of our term loans.gains.
Provision/(Benefit) for Income TaxesTax Expense
On December 22, 2017, the U.S. government enacted wide-ranging tax legislation, the Tax Cuts and Jobs Act (the "2017 Tax Act"). The 2017 Tax Act significantly revises U.S. tax law by, among other provisions, lowering the applicable U.S. federal statutory income tax rate from 35% to 21%, creating a partial territorial tax system that includes a mandatory one-time transition tax on previously deferred foreign earnings, and eliminating or reducing certain income tax deductions.
During the second quarter ended December 31, 2017, we recorded a one-time net charge of $46.0 million within our income tax provision as a provisional estimate of the net accounting impact of the 2017 Tax Act in accordance with Staff Accounting Bulletin No. 118 issued by the staff of the SEC ("SAB 118"), of which $48.7 million million related to the mandatory transition tax for deemed repatriation of deferred foreign income, $8.7 million of which we expect to pay over an 8-year period after considering the use of certain net operating losses and foreign tax credits, and certain limitations on executive compensation. The impact to our business resulting from the 2017 Tax Act, including related changes to our tax obligations and effective tax rate in future periods, as well as the one-time enactment-related charges recorded during the second quarter in fiscal 2018 on a provisional basis, are based on a reasonable estimate and are subject to change, and any change could differ materially from our current expectations. Further, there are certain effects of the 2017 Tax Act we cannot reasonably estimate as of the time of this filing, including (a) the Global Intangible Low Tax Income ("GILTI") rules, (b) the Foreign Derived Intangible Income ("FDII") deduction, (c) the Base Erosion Anti-Abuse Tax ("BEAT"), (d) provisions eliminating or reducing certain income tax deductions, such as interest expense, and certain employee expenses, and (e) the state tax impact of the 2017 Tax Act. As additional data is gathered, analyzed, and considered in context of the 2017 Tax Act and ASC 740, we may record additional or different tax charges in future periods during the measurement period.
Our provision for income taxes for the three months ended December 31, 20172023 was $49.9$24 million relative to earnings from continuing operationsloss before income taxes of $28.0$182 million. Our provision for income taxes for the three months ended December 31, 20162022 was $9.5$33 million relative to earnings from continuing operations before income taxes of $26.9$114 million. The income tax provisionexpense for the current periodquarter is not comparable toprimarily the same periodresult of the prior year due to the impact of the 2017 Tax Act, changesincome tax expense in pretax income over manyselect international jurisdictions and the impactinability to recognize income tax benefit on incremental domestic losses. The quarterly provision was also impacted by the geographic distribution of discrete items. Generally, fluctuations in the effective tax rate are primarily due to changes in our geographicCompany's pretax income resulting from our business mix, and changes in the tax impact of permanent differences, restructuring, other special items, certain equity related compensation, and other discrete tax items whichthat may have unique tax implications depending on the nature of the item.

Segment Review
The following charts depict the percentages of net revenue from each of our two reportable segments for the three months ended December 31, 2023 compared to the three months ended December 31, 2022. Refer below for discussions regarding each segment’s net revenue and EBITDA performance and to Non-GAAP Metrics” for a discussion of our use of Segment EBITDA, a measure that is not defined under U.S. GAAP.
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Segment ReviewMDA Circle Graph Q2FY24 v2.jpg
Our results on a segment basis for the three months ended December 31, 20172023 compared to the three months ended December 31, 20162022 were as follows:

Three Months Ended  
December 31,
FX ImpactConstant Currency Increase (Decrease)
(Dollars in millions)(Dollars in millions)20232022Change $Change %
Biologics
Net revenue
Net revenue
Net revenue$438 $580 $$(147)(25)%
Segment EBITDASegment EBITDA38 181 (144)(79)%
Pharma and Consumer Health
Net revenue
Net revenue
Net revenue587 570 11 %
Segment EBITDASegment EBITDA126 135 (12)(9)%
Three Months Ended  
 December 31,
 FX impact Constant Currency Increase/(Decrease)
(Dollars in millions)2017 2016 
 Change $ Change %
Softgel Technologies         
Inter-segment revenue elimination
Inter-segment revenue elimination
Inter-segment revenue elimination(1)(1)(1)100 %
Unallocated Costs (1)
Unallocated Costs (1)
(159)(52)(3)(104)*
Combined totals
Net revenue$228.1
 $201.9
 $7.1
 $19.1
 9%
Segment EBITDA50.1
 43.4
 1.1
 5.6
 13%
Drug Delivery Solutions         
Net revenue285.4
 214.0
 7.0
 64.4
 30%
Segment EBITDA81.1
 50.0
 2.0
 29.1
 58%
Clinical Supply Services         
Net revenue108.7
 77.0
 3.7
 28.0
 36%
Segment EBITDA19.0
 11.6
 1.0
 6.4
 55%
Inter-segment revenue elimination(15.9) (9.2) (0.8) (5.9) 64%
Unallocated costs (1)
(48.2) (19.8) (1.3) (27.1) *
Combined total         
Net revenue$606.3
 $483.7
 $17.0
 $105.6
 22%$1,024 $$1,149 $$15 $$(140)(12)(12)%
         
EBITDA from continuing operations$102.0
 $85.2
 $2.8
 $14.0
 16%
EBITDA from operations
EBITDA from operations
EBITDA from operations$$264 $$(260)(99)%
Change % calculations are based on amounts prior to rounding.
(1)    Unallocated costs includes equity-basedinclude restructuring and special items, stock-based compensation, certain acquisition-related costs, impairment charges, certain other corporate directed costs, and other costs that are not allocated to the segments as follows:
 Three Months Ended  
December 31,
(Dollars in millions)20232022
Impairment charges and gain/loss on sale of assets (a)
$(15)$(1)
Stock-based compensation(16)(10)
Restructuring and other special items (b)
(83)(33)
Pension settlement charges(3)— 
Goodwill impairment adjustments— 
Other expense (income), net (c)
(4)23 
Unallocated corporate costs, net(40)(31)
Total unallocated costs$(159)$(52)
(a)    Impairment charges and gain/loss on sale of assets during the three months ended December 31, 2023 include fixed asset impairment charges associated with equipment for a product with significant decline demand in our Biologics segment.
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 Three Months Ended  
 December 31,
(Dollars in millions)2017 2016
Impairment charges and gain/(loss) on sale of assets$(4.2) $(0.5)
Equity compensation(8.5) (4.9)
Restructuring and other special items (2)
(11.9) (7.2)
       Other income/(expense), net (3)
(13.6) 1.8
Non-allocated corporate costs, net(10.0) (9.0)
Total unallocated costs$(48.2) $(19.8)
(2)(b)    Restructuring and other special items during the three months ended December 31, 2023 include (i) restructuring charges associated with our plans to reduce costs, consolidate facilities, and optimize infrastructure across the organization and (ii) integration costs associated with our Metrics Contracts Services ("Metrics") acquisition. Restructuring and other special items during the three months ended December 31, 2022 include (i) restructuring charges associated with our plans to reduce costs, consolidate facilities, and optimize infrastructure across the organization and (ii) transaction and integration costs associated with the acquisitionour Metrics acquisition.
(c)    Refer to Note 7, Other Expense (Income), Net to our consolidated financial statements for details of Catalent Indiana.

(3) Amounts for the three months ended December 31, 2017 include $11.8 million of financing expenses related to the offering of the USD Notes and the Third Amendment and include a $6.1 million charge for commitment fees paid during the first quarter of fiscal 2018 on the Bridge Facility.

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amounts recorded within other expense, net in our Consolidated Financial Statements.
Provided below is a reconciliation of earnings/(loss) from continuing operationsnet loss to EBITDA from continuing operations:
 Three Months Ended  
December 31,
(Dollars in millions)20232022
Net (loss) earnings$(206)$81 
Depreciation and amortization121 103 
Interest expense, net66 47 
Income tax expense24 33 
EBITDA from operations$$264 
 Three Months Ended  
 December 31,
(Dollars in millions)2017 2016
Earnings/(loss) from continuing operations$(21.9) $17.4
Depreciation and amortization46.8
 35.5
Interest expense, net27.2
 22.8
Income tax expense/(benefit)49.9
 9.5
EBITDA from continuing operations$102.0
 $85.2

Softgel TechnologiesBiologics segment
2023 vs. 2022
Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic(25)%(79)%
Constant-currency change(25)%(79)%
Foreign exchange translation impact on reporting%— %
Total % change(24)%(79)%
 2017 vs. 2016
 Factors Contributing to Year-Over-Year ChangeThree Months Ended  
 December 31,
 Net Revenue Segment EBITDA
Revenue/Segment EBITDA without acquisitions / divestitures(3)% 4%
Impact of acquisitions12 % 9%
Constant currency change9 % 13%
Foreign currency translation impact on reporting4 % 2%
Total % change13 % 15%

Softgel Technologies’Biologics net revenue decreased by $147 million, or 25%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2022. The decrease was primarily driven by a decline in demand for COVID-19 related programs, partially offset by growth in our gene therapy offerings.

Biologics Segment EBITDA decreased by $144 million, or 79%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2022. The decrease, similar to that of net revenue, was primarily driven by a decline in demand for COVID-19 related programs as well as reduced productivity, an increase in inventory write-offs and higher costs due to increased spending on operational and engineering enhancements.
Pharma and Consumer Health segment
2023 vs. 2022
Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic%(9)%
Constant-currency change1 %(9)%
Foreign currency translation impact on reporting%%
Total % change%(6)%

Pharma and Consumer Health net revenue increased by $19.1$6 million, or 1%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2022. Net revenue increased 1% organically primarily driven by revenue from the manufacture of prescription products, partially offset by a decline in our consumer health products, primarily in our wellness products.
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Pharma and Consumer Health Segment EBITDA decreased $12 million, or 9%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2016. Net2022. The decrease, similar to that of net revenue, decreased 3%, excluding the impact of the Accucaps acquisition, primarilywas driven by decreased profit participation revenuean increase from the manufacture of 2% as comparedprescription products, partially offset by a decline in our consumer health products, primarily in our wellness products.
Six Months Ended December 31, 2023 Compared to threethe Six Months Ended December 31, 2022
The below tables summarize several financial metrics we use to measure performance for the six months ended December 31, 2016. Excluding the reduction in product participation revenue, net revenue without acquisitions decreased 1% primarily driven by decreased end-market volume demand for prescription products in Europe,2023 and lower end-market volume demand for consumer health products in Latin America and Asia Pacific, partially offset with revenue generated by a historical contractual settlement.
Softgel Technologies' Segment EBITDA increased by $5.6 million, or 13%, compared to the threesix months ended December 31, 2016, excluding the impact of foreign exchange. Segment EBITDA increased 4%, excluding the impact of the Accucaps acquisition. Excluding the reduction of product participation profit of 8%, segment EBITDA without acquisitions increased 12%, primarily related2022. Refer to the impactdiscussions below regarding performance and use of a historical contractual settlement of 6% and a favorable shift in product mix within our consumer health products in Asia Pacific and within our prescription products in North America.key financial metrics.
The net revenue and EBITDA impact to our Softgel Technologies segment from the Accucaps acquisition
287MDA Chart Graph Q2 YTD v9.jpg
Results for the threesix months ended December 31, 2017 was an increase of 12% and 9%, respectively,2023 compared to the prior-year period.
In December 2017, we divested of two manufacturing sites in Asia Pacific operated within the Softgel Technologies segment in order to better streamline our global operations. The site divestitures were material neither individually nor in aggregate to the segment or to the Company.
Drug Delivery Solutions segment
 2017 vs. 2016
 Factors Contributing to Year-Over-Year ChangeThree Months Ended  
 December 31,
 Net Revenue Segment EBITDA
Revenue/Segment EBITDA without acquisitions9% 18%
Impact of acquisitions21% 40%
Constant currency change30% 58%
Foreign currency translation impact on reporting3% 4%
Total % Change33% 62%

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Net revenue in our Drug Delivery Solutions segment increased by $64.4 million, or 30%, compared to the threesix months ended December 31, 2016, excluding the impact2022 were as follows:
 Six Months Ended  
December 31,
FX ImpactConstant Currency Increase (Decrease)
(Dollars in millions)20232022Change $Change %
Net revenue$2,006 $2,171 $33 $(198)(9)%
Cost of sales1,666 1,526 25 115 %
Gross margin340 645 (313)(48)%
Selling, general, and administrative expenses455 422 29 %
Goodwill impairment charges687 — — 687 *
Other operating expense36 25 — 11 35 %
Operating (loss) earnings(838)198 (1,040)*
Interest expense, net124 79 44 56 %
Other expense, net17 12 *
(Loss) earnings before income taxes(979)117 — (1,096)*
Income tax (benefit) expense(14)36 (51)(142)%
Net (loss) earnings$(965)$81 $(1)$(1,045)*
* Not meaningful
Change % calculations are based on amounts prior to rounding. 
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Net Revenue without acquisitions increased
2023 vs. 2022
Year-Over-Year ChangeSix Months Ended  
December 31,
Net Revenue
Organic(10)%
Impact of acquisitions%
Constant-currency change(9)%
Foreign currency translation impact on reporting%
Total % change(8)%
Net revenue decreased by 9%, driven primarily by timing of a standard maintenance shut-down at our European sterile pre-filled syringe facility of 6%, increased volume from our biologics offerings of 4%, partially offset by a decrease in product participation revenue of 1%.
Drug Delivery Solutions' segment EBITDA increased by $29.1$198 million, or 58%, compared to the three months ended December 31, 2016, excluding the impact of foreign exchange. Segment EBITDA without acquisitions increased by 18% primarily due to favorable absorption of cost and timing of a standard maintenance shut-down at our European sterile pre-filled syringe facility, increased volume from our biologics offerings, and a favorable shift in end-customer demand to certain higher margin offerings primarily in our U.S. operations within our oral delivery solutions platform. These increases were partially offset by operational inefficiencies with respect to products utilizing our blow-fill-seal technology platform, decreased profit from our analytical services platform driven by decreased sales volumes related to fee-for-service development work and analytical testing in the U.S., and a reduction in profit related to product participation.
The net revenue and EBITDA impact to our Drug Delivery Solutions segment from the Catalent Indiana acquisition for the three months ended December 31, 2017 was an increase of 21% and 40%, respectively, compared to the prior-year period.
Clinical Supply Services segment
 2017 vs. 2016
 Factors Contributing to Year-Over-Year ChangeThree Months Ended  
 December 31,
 Net Revenue Segment EBITDA
Revenue/Segment EBITDA without acquisitions36% 55%
Impact of acquisitions% %
Constant currency change36% 55%
Foreign currency translation impact on reporting5% 9%
Total % Change41% 64%
Clinical Supply Services' net revenue increased by $28.0 million, or 36%, compared to the three months ended December 31, 2016, excluding the impact of foreign exchange, primarily due to increased lower-margin comparator sourcing volume of approximately $17 million, or 22%, and higher volume and favorable mix in our storage and distribution business of approximately $13 million, or 16%.
Clinical Supply Services' segment EBITDA increased by $6.4 million, or 55%9%, excluding the impact of foreign exchange, compared to the threesix months ended December 31, 2016,2022. Net revenue decreased 10% organically on a constant-currency basis, primarily duerelated to increased sales volumes and favorable mixa significant decline in demand for COVID-19 related programs, partially offset by growth in our storage and distribution business, improved capacity utilization across the network, and increased profit from our lower-margin comparator sourcing.

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Six Months Ended December 31, 2017 Compared to the Six Months Ended December 31, 2016
 Six Months Ended  
 December 31,
 FX impact Constant Currency Increase/(Decrease)
(Dollars in millions)2017 2016 
 Change $ Change %
Net revenue$1,150.2
 $925.9
 $23.5
 $200.8
 22 %
Cost of sales822.7
 653.9
 18.8
 150.0
 23 %
Gross margin327.5
 272.0
 4.7
 50.8
 19 %
Selling, general and administrative expenses221.3
 194.4
 1.4
 25.5
 13 %
Impairment charges and (gain)/loss on sale of assets4.2
 0.5
 0.1
 3.6
 *
Restructuring and other1.3
 4.4
 
 (3.1) (70)%
Operating earnings100.7
 72.7
 3.2
 24.8
 34 %
Interest expense, net51.5
 44.9
 0.3
 6.3
 14 %
Other (income)/expense, net19.3
 (3.9) 2.3
 20.9
 *
Earnings from continuing operations, before income taxes29.9
 31.7
 0.6
 (2.4) (8)%
Income tax expense/(benefit)48.0
 9.7
 (0.3) 38.6
 *
Net earnings/(loss)$(18.1) $22.0
 $0.9
 $(41.0) *
 *Percentage not meaningful
Net Revenuegene therapy offerings.
Net revenue increased 1% inorganically as a result of acquisitions. We acquired Metrics Contract Services (“Metrics”) in October 2022.
Gross Margin
Gross margin decreased by $200.8$313 million, or 22%48%, compared to the six months ended December 31, 2016,2022, excluding the impact of foreign exchange. Net revenue increased 11% as a result of acquisitions. We acquired Pharmatek Laboratories, Inc. ("Pharmatek") in September 2016 and Catalent Indiana in October 2017, both within our Drug Delivery Solutions segment, and Accucaps in February 2017, within our Softgel Technologies segment. Excluding the impact of acquisitions, net revenue increased 11%,exchange, primarily due to an unfavorable shift in product mix, lower levels of utilization across the network, reduced productivity, and higher costs from increased volume in lower-margin comparator sourcingspending on operational and within our storage and distribution business within our Clinical Supply Services segment and favorable end customer demand for certain higher margin offerings within our oral delivery solutions platform and increased volume from our biologics offerings within our Drug Delivery Solutions segmentengineering enhancements in our U.S. operations.Biologics segment, partially offset by a decrease in inventory write-offs. On a constant-currency basis, gross margin, as a percentage of revenue, decreased 1,280 basis points to 16.8% in the six months ended December 31, 2023, compared to the corresponding prior-year period, primarily due to the factors described in the immediately preceding sentence.
Gross MarginSelling, General, and Administrative Expense
Gross margin
Selling, general, and administrative expense increased by $50.8$29 million or 19%7%, compared to the six months ended December 31, 2016,2022, excluding the impact of foreign exchange. Gross marginThe year-over-year increase was primarily driven by increased across all three reportable segments primarily due tospending on operational and engineering enhancements, a one-time insurance benefit of $10 million in the prior year, $6 million in net incremental expenses from businesses acquired in the last 12 months, and a $6 million increase sales volumes as discussed above. Onin stock-based compensation, partially offset by a constant currency basis, gross margin, as a percentage of revenue, decreased 70 basis points to 28.7%$2 million decline in integration costs.
Goodwill Impairment Charges
Goodwill impairment charges during the six months ended December 31, 2017 as compared2023 were associated with our Consumer Health and Biomodalities reporting units, which are part of our Pharma and Consumer Health and Biologics segments, respectively. For further details, see Note 4, Goodwill to 29.4% inour Consolidated Financial Statements.
Other Operating Expense
Other operating expense of $36 million for the prior-year period, primarily drivensix months ended December 31, 2023 increased by decreased product participation revenue within both our Softgel Technologies and our Drug Delivery Solutions segments and an unfavorable mix shift within our Softgel Technologies segment to lower-margin consumer health products as a result of the Accucaps acquisition, partially offset by a favorable mix shift to certain higher margin offerings within our oral delivery solutions and biologics offerings in our U.S. operations within our Drug Delivery Solutions segment.
Selling, General and Administrative Expense
Selling, general and administrative expense increased $25.5$11 million, or 13%35%, compared to the six months ended December 31, 2016,2022, excluding the impact of foreign exchange,exchange. The year-over-year increase was primarily driven by acquisition related expenses during the period, including one-time transaction fees of $10due to a $14 million related to the acquisition of Catalent Indianaincrease in October 2017fixed-asset impairment charges and an increase of approximately $11 million, which included approximately $6$3 million of incremental depreciation and amortizationpension settlement charges, partially offset by a $8 million decrease in restructuring charges.
Interest Expense, net
Interest expense, and $4 million incremental employee-related costs. Selling, general and administrative expenses further increased approximately $4 million for non-cash equity-based compensation driven by higher expense for certain performance based awards in the current period.

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Impairment charges and (gain)/loss on sale of assets
Impairment charges and loss on sale of assets of $4.2 million includes the loss on sale of two Softgel Technologies segment manufacturing sites in the Asia Pacific region. The site divestitures were material neither individually nor in aggregate to the segment or to the Company.
Restructuring and Other
Restructuring and other charges of $1.3$124 million for the six months ended December 31, 2017 decreased2023 increased by $3.1$44 million, or 56%, compared to the six months ended December 31, 2016. 2022, excluding the impact of foreign exchange. The increase was primarily attributable to higher interest rates on our variable rate debt and incremental borrowings.
For additional information concerning our debt and financing arrangements, including the changing mix of debt and equity in our capital structure, see “—Liquidity and Capital Resources” below and Note 5, Long-Term Obligations and Short-Term Borrowings to our Consolidated Financial Statements.
Other costs in the six months ended December 31, 2016 included claim resolution charges of $3.2 million (without regard to possible future insurance recoveries)Expense (Income), related to a previous temporary regulatory suspension at one of our manufacturing facilities. Restructuring expense will vary period to period based on the level of acquisitions during the year and site consolidation efforts to further streamline the business.
Interest Expense, net
Interest
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Other expense, net of $51.5$17 million for the six months ended December 31, 2017 increased $6.6 million compared to the six months ended December 31, 2016,2023 was primarily driven by an average higher levelforeign currency losses of outstanding debt associated with the financing for the Catalent Indiana acquisition in October 2017, offset by principal payments on our term loans and an overall reduction in our interest rates on our senior secured credit facility as compared to the prior year period.
On October 18, 2017, we completed the Debt Offering. Concurrent with the Debt Offering, we completed the Third Amendment, which lowered the interest rate on U.S. dollar-denominated and euro-denominated term loans and the revolving credit facility. The new applicable rate for U.S. dollar-denominated term loans decreased 0.50%, and the new applicable rate for euro-denominated term loans is LIBOR decreased 0.75%. The new applicable rate for the revolving loans decreased 1.25%.
Further, a component of the purchase price for the Catalent Indiana acquisition consists of $200 million in deferred purchase consideration payable in $50 million installments, on each anniversary of the closing date over a period of four years, which is accounted for as debt and includes a component of imputed interest expense.
On December 9, 2016, we completed the Euro Notes offering. The Euro Notes bear interest at the rate of 4.75% per annum and are payable semi-annually in arrears on June 15 and December 15 of each year.
Other (Income)/Expense, net$15 million.
Other expense, net of $19.3$2 million for the six months ended December 31, 2017 was primarily driven by $11.8 million of financing charges related to the Debt Offering and the Third Amendment and2022 includes a $6.1 million charge for commitment fees paid during the first quarter of fiscal 2018 on the Bridge Facility. Further, other expense, net for the six months ended December 31, 2017 includes $6.9 million of non-cash net losses from foreign exchange translation.miscellaneous non-operating expenses.
Other income, net for the six months ended December 31, 2016 of $3.9 million was primarily driven by non-cash net gains from foreign exchange translation recorded during the period of $7.5 million, partially offset by $4.3 million of financing charges in the prior year.Income Tax (Benefit) Expense
Provision/(Benefit) for Income Taxes
During the second quarter ended December 31, 2017, we recorded a one-time net charge of $46.0 million within our income tax provision as a provisional estimate of the net accounting impact of the 2017 Tax Act in accordance with SAB 118, of which $48.7 million million related to the mandatory transition tax for deemed repatriation of deferred foreign income, $8.7 million of which we expect to pay over an 8-year period after considering the use of certain net operating losses and foreign tax credits, and certain limitations on executive compensation. The impact to our business resulting from the 2017 Tax Act, including related changes to our tax obligations and effective tax rate in future periods, as well as the one-time enactment-related charges recorded during the second quarter in fiscal 2018 on a provisional basis, are based on a reasonable estimate and are subject to change, and any change could differ materially from our current expectations. Further, there are certain effects of the 2017 Tax Act we cannot reasonably estimate as of the time of this filing, including (a) the GILTI rules, (b) the FDII deduction, (c) the BEAT, (d)provisions eliminating or reducing certain income tax deductions, such as interest expense, and certain employee expenses, and (e) the state tax impact of the 2017 Tax Act. As additional data is gathered, analyzed, and considered in context of the 2017 Tax Act and ASC 740, we may record additional or different tax charges in future periods during the measurement period.
Our provisionbenefit for income taxes for the six months ended December 31, 20172023 was $48.0$14 million relative to earningsloss before income taxes of $29.9$979 million. Our provision for income taxes for the six months ended December 31, 20162022 was $9.7

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$36 million relative to earnings before income taxes of $31.7$117 million. The income tax provisionbenefit for the current period is not comparable toprimarily the same periodresult of the prior year due to the impact of the 2017 Tax Act, changesincome tax expense in pretax income over manyselect international jurisdictions and the impactinability to recognize income tax benefit on incremental domestic losses. The year to date benefit was also impacted by the geographic distribution of discrete items. Generally, fluctuations in the effective tax rate are primarily due to changes in our geographicCompany's pretax incomeloss resulting from our business mix, and changes in the tax impact of permanent differences, restructuring, other special items, certain equity related compensation, and other discrete tax items whichthat may have unique tax implications depending on the nature of the item.
Segment Review

The Company’sfollowing charts depict the percentage of net revenue for each of our two reportable segments for the six months ended December 31, 2023 compared to the six months ended December 31, 2022. Refer below for discussions regarding each segment’s net revenue and EBITDA performance and to Non-GAAP Metrics” for discussions of our use of Segment EBITDA and EBITDA from operations, measures that are not defined under U.S. GAAP.
MDA Circle Graph Q2FY24 YTD v2.jpg
Our results on a segment basis for the six months ended December 31, 20172023 compared to the six months ended December 31, 20162022 were as follows:
 Six Months Ended  
December 31,
FX ImpactConstant Currency Increase (Decrease)
(Dollars in millions)20232022Change $Change %
Biologics
Net revenue$886 $1,103 $10 $(227)(21)%
Segment EBITDA87 294 (208)(71)%
Pharma and Consumer Health
Net revenue1,1211,06923 29 %
Segment EBITDA227 243(22)(9)%
Inter-segment revenue elimination(1)(1)— — *
Unallocated Costs (1)
(936)(139)(4)(793)*
Combined totals
Net revenue$2,006 $2,171 $33 $(198)(9)%
(Loss) EBITDA from operations$(622)$398 $$(1,023)*
 Six Months Ended  
 December 31,
 FX impact Constant Currency Increase/(Decrease)
(Dollars in millions)2017 2016 
 Change $ Change %
Softgel Technologies         
Net revenue$447.8
 $388.3
 $11.1
 $48.4
 12%
Segment EBITDA85.2
 73.9
 1.2
 10.1
 14%
Drug Delivery Solutions         
Net revenue511.2
 405.3
 9.5
 96.4
 24%
Segment EBITDA128.5
 92.0
 2.3
 34.2
 37%
Clinical Supply Services         
Net revenue218.4
 152.0
 4.1
 62.3
 41%
Segment EBITDA35.7
 22.1
 1.1
 12.5
 57%
Inter-segment revenue elimination(27.2) (19.7) (1.2) (6.3) 32%
Unallocated costs (1)
(82.2) (40.1) (2.3) (39.8) 99%
Combined total         
Net revenue$1,150.2
 $925.9
 $23.5
 $200.8
 22%
          
EBITDA from continuing operations$167.2
 $147.9
 $2.3
 $17.0
 11%
     *Percentage not meaningful
(1)Unallocated costs includes equity-based compensation, certain acquisition-related costs, impairment charges, and certain other costs that are not allocated to the segments as follows:
 Six Months Ended  
 December 31,
(Dollars in millions)2017 2016
Impairment charges and gain/(loss) on sale of assets$(4.2) $(0.5)
Equity compensation(15.5) (11.8)
Restructuring and other special items (2)
(24.2) (13.1)
       Other income/(expense), net (3)
(19.3) 3.9
Non-allocated corporate costs, net(19.0) (18.6)
Total unallocated costs$(82.2) $(40.1)
(2)Restructuring and other special items include transaction and integration costs associated with the acquisition of Catalent Indiana.

Change % calculations are based on amounts prior to rounding.
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*Percentage not meaningful
(3)Amounts for the six months ended December 31, 2017 include $11.8 million of financing expenses related to the offering of the USD Notes and the Third Amendment and include a $6.1 million charge for commitment fees paid during the first quarter of fiscal 2018 the Bridge Facility.
(1) Unallocated costs include restructuring and special items, stock-based compensation, goodwill impairment charges, fixed asset impairment charges, certain other corporate-directed costs, and other costs that are not allocated to the segments as follows:
 Six Months Ended  
December 31,
(Dollars in millions)20232022
Impairment charges and gain/loss on sale of assets (a)
$(14)$
Stock-based compensation(35)(29)
Restructuring and other special items (b)
(106)(42)
Pension settlement charges(3)— 
Goodwill impairment charges (c)
(687)— 
       Other expense, net (d)
(17)(2)
Non-allocated corporate costs, net(74)(67)
Total unallocated costs$(936)$(139)
(a) Impairment charges and gain/loss on sale of assets during the six months ended December 31, 2023 include fixed-asset impairment charges associated with equipment for a product with significant decline demand in our Biologics segment.
(b) Restructuring and other special items during the six months ended December 31, 2023 include (i) restructuring charges associated with our plans that reduced costs, consolidated facilities, and optimized our infrastructure across the organization, most notably the announced closure of our San Francisco facility and (ii) transaction and integration costs associated with the Metrics acquisition.
Restructuring and other special items during the six months ended December 31, 2022 include (i) restructuring charges associated with our plans to reduce costs, consolidate facilities, and optimize our infrastructure across the organization, (ii) transaction and integration costs associated with the Metrics acquisition and (iii) warehouse exit costs for a product we no longer manufacture in our Pharma and Consumer Health segment.
(c)    Goodwill impairment charges during the six months ended December 31, 2023 were associated with our Consumer Health and Biomodalities reporting units, which are part of our Pharma and Consumer Health and Biologics segments, respectively. For further details, see Note 4, Goodwill to our Consolidated Financial Statements.
(d)    Refer to Note 7, Other Expense (Income), Net to our consolidated financial statementsfor details.

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Provided below is a reconciliation of earnings/(loss) from continuing operationsnet earnings to EBITDA from continuing operations:
 Six Months Ended  
December 31,
(Dollars in millions)20232022
Net (loss) earnings$(965)$81 
Depreciation and amortization233 202 
Interest expense, net124 79 
Income tax (benefit) expense(14)36 
(Loss) EBITDA from operations$(622)$398 
Biologics segment
2023 vs. 2022
Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic(21)%(71)%
Constant-currency change(21)%(71)%
Foreign exchange translation impact on reporting%%
Total % change(20)%(70)%
 Six Months Ended  
 December 31,
(Dollars in millions)2017 2016
Earnings/(loss) from continuing operations$(18.1) $22.0
Depreciation and amortization85.8
 71.3
Interest expense, net51.5
 44.9
Income tax (benefit)/expense48.0
 9.7
EBITDA from continuing operations$167.2
 $147.9
Softgel TechnologiesNet revenue in our Biologics segment
 2017 vs. 2016
 Factors Contributing to Year-Over-Year ChangeSix Months Ended  
 December 31,
 Net Revenue Segment EBITDA
Revenue/Segment EBITDA without acquisitions(1)% 1%
Impact of acquisitions13 % 13%
Constant currency change12 % 14%
Foreign exchange fluctuation3 % 1%
Total % Change15 % 15%
Softgel Technologies’ net revenue increased $48.4 decreased by $227 million, or 12%21%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2016. Net revenue decreased 1%, excluding the impact of the Accucaps acquisition,2022. The decrease was primarily driven by decreased profit participation revenue of 1% as compared to six months ended December 31, 2016.
Softgel Technologies' Segment EBITDA increased by $10.1 million, or 14%, compared to the six months ended December 31, 2016, excluding the impact of foreign exchange. Segment EBITDA increased 1% excluding the impact of the Accucaps acquisition. Excluding the reduction of product participation profit of 5%, segment EBITDA without acquisitions increased 6%, primarily related to the impact of a historical contractual settlement of 4% and a favorable shiftsignificant decline in product mix within our prescription products in North America.
Net revenue and Segment EBITDA in our Softgel Technologies segment increased in the six months ended December 31, 2017 compared to the six months ended December 31, 2016 by 13% and 13%, respectively, due to the Accucaps acquisition.
In December 2017, we divested of two manufacturing sites in Asia Pacific operated within the Softgel Technologies segment in order to better streamline our global operations. The site divestitures were material neither individually nor in aggregate to the segment or to the Company.


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Drug Delivery Solutions segment
 2017 vs. 2016
 Factors Contributing to Year-Over-Year ChangeSix Months Ended  
 December 31,
 Net Revenue Segment EBITDA
Revenue/Segment EBITDA without acquisitions11% 14%
Impact of acquisitions13% 23%
Constant currency change24% 37%
Foreign exchange fluctuation2% 3%
Total % Change26% 40%
Net revenue in our Drug Delivery Solutions segment increased by $96.4 million, or 24%, compared to the six months ended December 31, 2016, excluding the impact of foreign exchange. Revenue without acquisitions increased by 11%, driven primarily by favorable end customer demand for certain higher margin offerings primarily in our U.S. operations within our oral delivery solutions platform of 5%, increased volume from our biologics offerings of 4% and by timing of executionCOVID-19 related to timing of a standard maintenance shut-down at our European sterile pre-filled syringe facility of 2%.
Drug Delivery Solutions' Segment EBITDA increased by $34.2 million, or 37%, compared to the six months ended December 31, 2016, excluding the impact of foreign exchange. Segment EBITDA without acquisitions increased by 14%, primarily due to an increase in sales volumes driven by favorable end-customer demand for certain higher margin offerings primarily in our U.S. operations within our oral delivery solutions platform of 11%, increased volume from our biologics offerings of 10%, and favorable absorption of cost and timing of a standard maintenance shut-down at our European sterile pre-filled syringe facility of 5%. Segment EBITDA also increased as a result of increased profit from our San Diego site (obtained as part of the Pharmatek acquisition) lapping a full year of ownership. These increases wereprograms, partially offset by operational inefficiencies with respect to products utilizing our blow-fill-seal technology platform of 10%, decreased profit from our analytical services platform driven by decreased sales volumes related to fee-for-service development work and analytical testing in the U.S. of 6%.
On September 22, 2016, we acquired Pharmatek, which increased net revenue and EBITDAstrong growth in our Drug Delivery Solutions segment for the six months ended December 31, 2017gene therapy offerings.
Biologics Segment EBITDA decreased by 2% and 1%, respectively, compared to the corresponding prior-year period.
On October 23, 2017, we acquired Catalent Indiana which increased net revenue and EBITDA in our Drug Delivery Solutions segment for the six months ended December 31, 2017 by 11% and 22%, respectively, compared to the corresponding prior-year period.
Clinical Supply Services segment
 2017 vs. 2016
 Factors Contributing to Year-Over-Year ChangeSix Months Ended  
 December 31,
 Net Revenue Segment EBITDA
Revenue/Segment EBITDA without acquisitions41% 57%
Impact of acquisitions% %
Constant currency change41% 57%
Foreign exchange fluctuation3% 5%
Total % Change44% 62%
Clinical Supply Services' net revenue increased by $62.3$208 million, or 41%, compared to the six months ended December 31, 2016, excluding the impact of foreign exchange, primarily due to increased lower-margin comparator sourcing volume of approximately $35 million, or 23%, and higher volume related to our storage and distribution business of approximately $27 million, or 18%.
Clinical Supply Services' Segment EBITDA increased by $12.5 million, or 57%71%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2016,2022. Segment EBITDA decreased 71%, compared to the six months ended December 31, 2022, excluding the impact of acquisitions. The decrease was primarily driven by a significant decline in demand for COVID-19 related programs, lower levels of utilization across the Biologics network, and higher costs due to increased sales volumesspending on operational and engineering enhancements, which were partially offset by strong growth in our storagegene therapy offerings and a decrease in inventory write-offs.

Pharma and Consumer Health segment
2023 vs. 2022
Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic— %(13)%
Impact of acquisitions%%
Constant-currency change3 %(9)%
Foreign exchange translation impact on reporting%%
Total % change%(6)%

Pharma and Consumer Health net revenue increased $29 million, or 3%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2022. Organic revenue was flat when compared to the six months ended December 31, 2022. The increase in revenue from the manufacture of prescription products and growth in our clinical supply services, were partially offset by a decline in demand for our consumer health products, primarily our wellness products.
Pharma and Consumer Health Segment EBITDA decreased $22 million, or 9%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2022. Segment EBITDA decreased 13%, compared to the six months ended December 31, 2022, excluding the impact of acquisitions. The decrease in organic Segment EBITDA was primarily driven by a decline in demand for our consumer health products, partially offset by an increase in revenue from the manufacture of prescription products.
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We acquired Metrics in October 2022, which increased the segment's net revenue and Segment EBITDA on an inorganic basis by 3% and 4%, respectively, in the six months ended December 31, 2023, compared to the corresponding prior-year period.
distribution business, improved capacity utilization across the network, as well as increased profit from our lower-margin comparator sourcing.
Liquidity and Capital Resources
Sources and Uses of Cash
Our principal sourcesources of liquidity hashave been cash flows generated from operations and certain financing activities for acquisitions.occasional capital market activities. The principal uses of cash are to fund planned operating and capital expenditures, business or asset acquisitions, interest payments on our debt, and any mandatory or discretionary principal paymentspayment on debt issuances.our debt. As of December 31, 2017,2023, Catalent Pharma Solutions, Inc., our financing needs were supported by the five-year, $200 millionprincipal operating subsidiary (“Operating Company”), had available $1.09 billion in borrowing capacity under our revolving credit facility, maintained by Catalent Pharma Solutions, Inc. (our "Operating Company") that matures in May 2022 (following the Third Amendment in October 2017), the capacity of which is reduced by $13.0due to $6 million in outstanding letters of credit. The revolving credit facility includes borrowing capacity available for letters of credit and for short-term borrowings, referred tooutstanding as swing-line borrowings. As of December 31, 2017, we had no outstanding2023.
We believe that our cash on hand, cash from operations, and available borrowings under our revolving credit facility.
On October 29, 2015,facility will be adequate to meet our Board of Directors authorized a share repurchase program to use up to $100.0 million to repurchase shares of our outstanding common stock. Underliquidity needs for at least the program, we are authorized to repurchase shares through open market purchases, privately negotiated transactions or otherwise as permitted by applicable federal securities laws. There has been no purchase pursuant to this program as of December 31, 2017.
U.S. Tax Reform Considerations

Recent changes to the taxation of undistributed foreign earnings in connection with the 2017 Tax Act could potentially change our future intentions regarding the reinvestment of such earnings. We intend to continue to monitor regulatory developments concerning the taxation of undistributed foreign earnings,next 12 months, as well as the amounts expected to become due with respect to our liquidity needs both domestic and foreign. If our plans change and we choose to repatriate any funds to the U.S. in the future, we could potentially be subject to applicable state, local, and/or foreign taxes. We have yet to determine the potential use of any cash that may be repatriated to the U.S. as a result of the 2017 Tax Act. Based on the current estimate of the mandatory transition cash tax liability of $8.7 million and timing of the related payments, we believe that cash from operations will be sufficient to make all required payments.pending capital projects.
Cash Flows
The following table summarizes our consolidated statementstatements of cash flows:
 Six Months Ended  
 December 31,
  
(Dollars in millions)2017 2016 Difference
Net cash provided by/(used in):     
Operating activities$176.0
 $96.0
 $80.0
Investing activities$(825.7) $(138.5) $(687.2)
Financing activities$682.4
 $175.7
 $506.7
 Six Months Ended  
December 31,
 
(Dollars in millions)20232022$ Change
Net cash provided by (used in):
Operating activities$42 $122 $(80)
Investing activities$(179)$(724)$545 
Financing activities$84 $597 $(513)
Operating Activities

For the six months ended December 31, 2017,2023, cash provided by operating activities operations was $176.0$42 million compared to $96.0$122 million for the corresponding prior-year period. Cash flow from operating activitiesin cash provided by operations for the six months ended December 31, 2017 increased2022. The year-over-year change was primarily due to certaina benefit in working capital improvements primarily drivenpartially offset by a decrease in trade receivablesoperating earnings and an increase in interest payments due to higher outstanding debt balances and higher rates on our variable rate debt. The lump-sum payments from the higher collectionpartial settlement of receivables during the current-year six-month period compared tofrozen domestic pension plan were made with cash from the prior-year period.qualified pension plans, not with Company cash.
Investing Activities
For the six months ended December 31, 2017,2023, cash used in investing activities was $825.7$179 million, compared to $138.5$724 million for the six months ended December 31, 2016, primarily driven by $748.0 million of cash paid for the acquisition of Catalent Indiana in the second quarter of fiscal 2018. During the prior-year six-month period, $86.9 million of cash was paid for the acquisition of Pharmatek, net of cash acquired.2022. The increasedecrease in cash used in investing activities was also due to an increaseprimarily driven by a decrease in mergers and acquisitions activity and a decrease in acquisition of property, plantequipment, and equipment, which totaled $82.9 million for the six months ended December 31, 2017 compared to $54.1 million inother productive assets.
Financing Activities
For the six months ended December 31, 2016.

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Financing Activities
For the six months ended December 31, 2017,2023, cash provided by financing activities was $682.4$84 million, compared to $175.7cash provided by financing activities of $597 million for the six months ended December 31, 2016,2022. The decrease in cash provided by financing activities was primarily driven by a $500 million decrease in net proceeds of $442.6 million and $277.8 million raised as part of our Debt Offering and a primary offering of our common stock in September 2017 (the "Equity Offering"), respectively, during the current-year six-month period. In the Equity Offering, we sold 7.4 million shares of our common stock at a price of $39.10 per share, before underwriting discounts and commissions. The net proceeds of $277.8 million includes the effect of these discounts and commissions and other offering expenses. The net proceeds of these offerings were used to fund a portion of the initial consideration for the Catalent Indiana acquisition. Contemporaneous to completing the Debt Offerings, we completed the Third Amendment to lower the interest rate and extend the maturity dates on our senior secured credit facilities. In connection with the Debt Offering and the Third Amendment, we incurred $22.8 million of debt discount and third-party financing costs, of which $11.8 million was expensed and recorded in other expense/(income), net in the consolidated statement of operations.borrowings.
Guarantees and Security
Senior Secured Credit Facilities
All obligations under the Credit Agreement and the guarantees of those obligations are secured by substantially all of the following assets of Operating Company and each guarantor (Operating Company's parent entity, PTS Intermediate Holdings LLC ("PTS Intermediate"), and each of Operating Company's material domestic subsidiaries), subject to certain exceptions:
a pledge of 100% of the capital stock of Operating Company and 100% of the equity interests directly held by Operating Company and each guarantor in any wholly owned material subsidiary of Operating Company or any guarantor (which pledge, in the case of any non-U.S. subsidiary of a U.S. subsidiary, will not include more than 65% of the voting stock of such non-U.S. subsidiary); and
a security interest in, and mortgages on, substantially all tangible and intangible assets of Operating Company and of each guarantor, subject to certain limited exceptions.
The Euro Notes and the USD Notes
All obligations under the Euro Notes and the USD Notes are general, unsecured and subordinated to all existing and future secured indebtedness of the guarantors to the extent of the value of the assets securing such indebtedness. The Euro Notes and the USD Notes are each separately guaranteed by all of Operating Company's wholly owned U.S. subsidiaries that guarantee the senior secured credit facilities. Neither the Euro Notes nor the USD Notes are guaranteed by either PTS Intermediate or Catalent, Inc.
Debt Covenants
Senior Secured Credit Facilities
The Credit Agreement contains a number of covenants that, among other things, restrict, subject to certain exceptions, Operating Company’sour (and Operating Company’sour restricted subsidiaries’) ability to incur additional indebtedness or issue certain preferred shares; create liens on assets; engage in mergers and consolidations; sell assets; pay dividends and distributions or repurchase capital stock; repay subordinated indebtedness; engage in certain transactions with affiliates; make investments, loans, or advances; make certain acquisitions; enter into sale and leaseback transactions; amend material agreements governing Operating Company’sour subordinated indebtednessindebtedness; and change Operating Company’sour lines of business.
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The Credit Agreement also contains change of controlchange-of-control provisions and certain customary affirmative covenants and events of default. The revolving credit facility requires compliance with a net leverage covenant when there is a 30% or more draw outstanding at a period end. As of December 31, 2017,2023, we were in compliance with all material covenants related to our senior-secured obligations.under the Credit Agreement.
Subject to certain exceptions, the Credit Agreement permits us and our restricted subsidiaries to incur certain additional indebtedness, including secured indebtedness. None of our non-U.S. subsidiaries or our Puerto Rico subsidiariessubsidiary is a guarantor of the loans.
As market conditions warrant,On November 22, 2023, Operating Company, entered into Amendment No. 10 to the Credit Agreement, which further extended the deadlines by which we are required to deliver to the administrative agent (i) our audited financial statements as at the end of and for the fiscal year ended June 30, 2023, together with the auditor’s report and opinion on such audited financial statements, to January 26, 2024, and (ii) our affiliates may from timeunaudited financial statements as at the end of and for the fiscal quarter ending September 30, 2023 to time seekMarch 13, 2024.

On December 19, 2023, Operating Company entered into Amendment No. 11 to purchasethe Credit Agreement, pursuant to which Operating Company incurred $600 million aggregate principal amount of new incremental dollar term loans.
Under the Credit Agreement, our outstanding debtability to engage in privately negotiated or open market transactions, by tender offer or otherwise. Subjectcertain activities such as incurring certain additional indebtedness, making certain investments, and paying certain dividends is tied to any applicable limitation containedratios based on Adjusted EBITDA (which is defined as “Consolidated EBITDA” in the Credit Agreement). Adjusted EBITDA is based on the definitions in the Credit Agreement, any purchase made by us may be funded by the use of cash on our balance sheet or the incurrence of new secured or unsecured debt. is not defined under U.S. GAAP, and is subject to important limitations.
The amounts involved in any such purchase transactions, individually or in the aggregate, may be material. Any such purchase may be with respect to a substantial amount of a particular class orSenior Notes
The several indentures governing each series of debt, withour outstanding senior notes (collectively, the

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attendant reduction in the trading liquidity of such class or series. In addition, any such purchases made at prices below the “adjusted issue price” (as defined for U.S. federal income tax purposes) may result in taxable cancellation of indebtedness income to us, which amounts may be material, and in related adverse tax consequences to us.
The Euro Notes and the USD Notes
The Indentures governing the Euro Notes and the USD Notes (the "Indentures" “Indentures”) contain certain covenants that, among other things, limit theour ability of Operating Company and its restricted subsidiaries to incur or guarantee more debt or issue certain preferred shares,shares; pay dividends on, repurchase, or make distributions in respect of their capital stock or make other restricted payments,payments; make certain investments,investments; sell certain assets,assets; create liens,liens; consolidate, merge, sellsell; or otherwise dispose of all or substantially all of their assets,assets; enter into certain transactions with their affiliates, and designate their subsidiaries as unrestricted subsidiaries. These covenants are subject to a number of exceptions, limitations, and qualifications as set forth in the Indentures. The Indentures also contain customary events of default, including, but not limited to, nonpayment, breach of covenants, and payment or acceleration defaults in certain other indebtedness of Operating Company or certain of its subsidiaries. Under the Indentures, uponUpon an event of default, either the holders of at least 30% in principal amount of eithereach of the then-outstanding Euroseries of Senior Notes, or the then-outstanding USD Notes, or either of the Trusteesapplicable Trustee under the applicable notesIndentures, may declare the applicable senior notes immediately due and payable,payable; or in certain circumstances, the applicable senior notes automatically will become automatically immediately due and immediately payable. As of December 31, 2017, we were2023, Operating Company was in compliance with all material covenants related tounder the Indentures.

Capital Resources
As market conditions warrant, we and our affiliates may from time to time seek to purchase our outstanding debt in privately negotiated or open-market transactions, by tender offer or otherwise. Subject to any applicable limitation contained in the Credit Agreement, any purchase made by us may be funded by the use of cash on hand or the incurrence of new secured or unsecured debt. The amounts involved in any such purchase transaction, individually or in the aggregate, may be material. Any such purchase may be with respect to a substantial amount of a particular class or series of debt, with the attendant reduction in the trading liquidity of such class or series. In addition, any such purchase made at prices below the “adjusted issue price” (as defined for U.S. federal income tax purposes) may result in taxable cancellation of indebtedness income to us, which amounts may be material, or in related adverse tax consequences to us.
Geographic Allocation of Cash
As of December 31, 20172023 and June 30, 2017, the amounts of2023, our non-U.S. subsidiaries held cash and cash equivalents held by foreign subsidiaries were $272.2of $176 million and $249.8$181 million, respectively, out of the total consolidated cash and cash equivalents of $329.5$229 million and $288.3$280 million, respectively. These balances are dispersed across many international locations around the world.

Backlog
While we generally have long-term supply agreements that provide for a revenue stream over a period of years, our backlog represents, as of a point in time, future service revenues from work not yet completed. For our Softgel Technologies and Drug Delivery Solutions segments, backlog represents firm orders for manufacturing services and includes minimum volumes, where applicable. For our Clinical Supply Services segment, backlog represents estimated future service revenues from work not yet completed under signed contracts. Using these methods of reporting backlog, as of December 31, 2017, backlog was approximately $1,121.6 million, compared to approximately $1,052.2 million as of June 30, 2017, including approximately $306.0 million and $338.3 million, respectively, related to our Clinical Supply Services segment. We expect to recognize approximately 70% of revenue from the backlog in existence as of December 31, 2017 by June 30, 2018.
To the extent projects are delayed, the timing of our revenue could be affected. If a customer cancels an order, we may be reimbursed for the costs we have incurred. For orders that are placed inside a contractual firm period, we generally have a contractual right to payment in the event of cancellation. Fluctuations in our reported backlog levels also result from the timing and order pattern of our customers who often seek to manage their level of inventory on hand. Because of customer ordering patterns, our backlog reported for certain periods may fluctuate and may not be indicative of future results.
Interest Rate Risk Management
A portion of the debt used to finance our operations is exposed to interest-rate fluctuations. We may use various hedging strategies and derivative financial instruments to create an appropriate mix of fixed- and floating-rate assets and liabilities. Historically,In February 2021, we have usedentered into an interest-rate swaps to manageswap agreement with Bank of America N.A. that acts as a hedge against the economic effect of variable rate interest obligationsa portion of the variable-interest obligation associated with our floating-rateU.S. dollar-denominated term loans under our senior secured credit facilities, so that the interest payable on that portion of the term loans effectivelydebt becomes fixed at a certain rate, thereby
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reducing the impact of future interest-rate changes on our future interest expense. AsThe applicable rate for the U.S. dollar-denominated term loan under the Credit Agreement was LIBOR (subject to a floor of 0.50%) plus 2.00% as of December 31, 2017, we did not have any2023; however, as a result of this interest-rate swap agreements in place that would have the economic effect of modifyingagreement, the variable portion of the applicable rate on $500 million of the term loan was effectively fixed at 0.9985%.
To conform with the adoption of ASC 848, Reference Rate Reform and the Eighth Amendment, the Company amended the 2021 Rate Swap as the 2023 Rate Swap. The 2023 Rate Swap continues to effectively fix the rate of interest obligations associated withpayable on the same portion of our floating-rateU.S dollar-denominated term loans.loans under our secured credit facilities. The applicable rate for the U.S. dollar-denominated term loan under the Credit Agreement was SOFR (subject to a floor of 0.39%) plus 2.00% as of December 31, 2023. As a result of the 2023 Rate Swap, the variable portion of the applicable interest rate on $500 million of the U.S. dollar-denominated term loans is now effectively fixed at 0.9431%.
Currency Risk Management
We are exposed to fluctuations in the Euro-USDeuro-U.S. dollar exchange rate on our investments in our operations in Europe. While we do not actively hedge against changes in foreign currency, we have mitigated the exposure of our investments in our European operations by denominating a portion of our debt in euros. At December 31, 2017,2023, we had $811.9$910 million of euro-denominated debt outstanding that qualifies as a hedge of a net investment in foreignEuropean operations. Refer to Note 9, Derivative Instruments and Hedging Activities,to our unaudited consolidated financial statements included elsewhere in this Quarterly Report on Form 10-QConsolidated Financial Statements for further discussion of net investment hedge activity in the period.
Periodically,From time to time, we may utilizeuse forward foreign currency exchange contracts to manage our exposure to the variability of cash flows primarily related to the foreign exchange rate changes of future foreign currency transaction costs. In addition, we may utilize

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foreign currency forwarduse such contracts to protect the value of existing foreign currency assets and liabilities. Currently, we do not utilizeuse any forward foreign currency exchange contracts. We expect to continue to evaluate hedging opportunities for foreign currency in the future.

Contractual Obligations
Besides the changes in our long-term obligations related to the Third Amendment, the offering of the USD Notes, and the deferred purchase consideration associated with the Catalent Indiana acquisition as disclosed in Liquidity and Capital Resources earlier in this Item, there has been no significant change to our contractual obligations since our Annual Report on Form 10-K for the period ended June 30, 2017. Refer to Note 10 to our unaudited consolidated financial statements included elsewhere in this Quarterly Report on Form 10-Q for a further discussion regarding tax reform and the Company's long-term obligations.
Off-Balance Sheet Arrangements
Other than short-term operating leases and outstanding letters of credit as discussed above, we do not have any material off-balance sheet arrangementsarrangement as of December 31, 2017.2023.


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Item 3.QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
We are exposed to cash flowITEM 3.    QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
For a discussion of our quantitative and earnings fluctuations as a result of certain market risks. Thesequalitative disclosures about market risks, primarily relate to changessee the section titled Item 7A, Quantitative and Qualitative Disclosures About Market Risks in interest rates associated with our long-term debt obligations and foreign exchange rate changes.
Interest Rate Risk
The Company has historically used interest-rate swaps to manage the economic effect of variable rate interest obligations associated with our floating-rate term loans so that the interest payable on the term loans effectively becomes fixed at a certain rate, thereby reducing the impact of future interest-rate changes on our future interest expense.Fiscal 2023 10-K. As of December 31, 2017, we did not have any interest-rate swap agreements2023, there has been no material change in place that would either have the economic effect of modifying the variable interest obligations associated with our floating-rate term loans or would be considered an effective cash flow hedge for financial reporting purposes.
Foreign Currency Exchange Risk
By the nature of our global operations, we are exposed to cash flow and earnings fluctuations resulting from foreign exchange rate variation. These exposures are transactional and translational in nature. Since we manufacture and sell our products throughout the world, our foreign currency risk is diversified. Principal drivers of this diversified foreign exchange exposure include the European euro, British pound, Argentinean peso, Brazilian real and Australian dollar. Our transactional exposure arises from the purchase and sale of goods and services in currencies other than the functional currency of our operational units. We also have exposure related to the translation of financial statements of our foreign subsidiaries into U.S. dollars, the functional currency of the parent. The financial statements of our operations outside the U.S. are measured using the local currency as the functional currency. Adjustments to translate the assets and liabilities of these foreign operations in U.S. dollars are accumulated as a component of other comprehensive income/(loss) utilizing period-end exchange rates. Foreign currency transaction gains and losses calculated by utilizing weighted average exchange rates for the period are included in the statements of operations in “other (income)/expense, net.” Such foreign currency transaction gains and losses include inter-company loans denominated in non-U.S. dollar currencies.

information.
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Item 4.CONTROLS AND PROCEDURES
ITEM 4.    CONTROLS AND PROCEDURES
Disclosure Controls and Procedures

We maintain disclosure controls and procedures that are designed to ensure that information required to be disclosed in our reports under the Exchange Act is recorded, processed, summarized, and reported within the time periods specified in the SEC’s rules and forms, and that such information is accumulated and communicated to our management, including our President and Chief Executive Officer and our Executive Vice President and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosures. Any control or procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving the desired control objectives. Our management, with the participation ofincluding our President and Chief Executive Officer and our Executive Vice President and Chief Financial Officer, has evaluated the effectiveness of the design and operation of our disclosure controls and procedures as of the end of the period covered by this Quarterly Report on Form 10-Q. Based upon that evaluation, our President and Chief Executive Officer and our Executive Vice President and Chief Financial Officer concluded that, as of December 31, 2017,2023, our disclosure controls and procedures were not effective to accomplish their objectives at the reasonable assurance level.level, as a result of the material weaknesses in our internal control over financial reporting disclosed below.
Material Weaknesses in Internal Control over Financial Reporting
A material weakness (as defined in Rule 12b-2 under the Exchange Act) is a deficiency, or a combination of deficiencies, in internal controls over financial reporting such that there is a reasonable possibility that a material misstatement of our annual or interim consolidated financial statements will not be prevented or detected on a timely basis.

Material Weakness in Internal Controls over Financial Reporting – Contract Modifications

In connection with our evaluation for the three months ended December 31, 2023, we identified a material weakness in internal control over financial reporting as we did not maintain effective internal controls to properly identify and assess the accounting treatment of contract modification arrangements under ASC 606, Revenue from Contracts with Customers. The review of the accounting assessments for certain modified contracts during the quarter ended December 31, 2023, was not performed with the necessary level of technical competency to detect a material misstatement.

Material Weakness in Internal Controls over Financial Reporting – Income Tax Provision

In connection with our evaluation for the three months ended December 31, 2023, we identified a material weakness in internal control over financial reporting as we did not maintain effective internal control over the preparation and review of the interim income tax provision. Specifically, the Company did not design an appropriate interim review control over the completeness and accuracy of certain inputs to the quarterly income tax provision calculations. While the control deficiency did not result in a material misstatement to the Company’s interim consolidated financial statements, there is a reasonable possibility that the control deficiency could have resulted in a material misstatement of the income tax related accounts or disclosures in the Company’s interim consolidated financial statements that would not have been prevented or detected on a timely basis.

Previously Disclosed Material Weakness in Internal Controls over Financial Reporting – Revenue Recognition

As previously disclosed, management identified during the preparation of our unaudited consolidated financial statements for the fiscal year ended June 30, 2023 a material weakness in our internal controls over financial reporting relating to the year ended June 30, 2022, which remains unremediated as of December 31, 2023.

We did not maintain effective controls over the appropriateness of revenue recognition related to modifications of customer agreements at our Bloomington, Indiana facility. Specifically, we did not maintain effective controls to properly identify and assess the accounting treatment of modifications to arrangements that were accounted for under ASC 606, Revenue from Contracts with Customers. The reviewer had insufficient knowledge of the requirements of the ASC 606 revenue recognition accounting model, and therefore the review procedures were not performed with the necessary level of competence to prevent or detect a material misstatement on a timely basis.

Furthermore, the compensating control to review the accounting assessments for contract modifications was not sufficiently designed to detect accounting misstatements. As previously disclosed, this control deficiency resulted in an immaterial revision to our consolidated financial statements for the fiscal year ended June 30, 2022 to correct an overstatement of revenue of $26 million. While this control deficiency did not result in a material misstatement of our consolidated financial statements, there is a reasonable possibility that this deficiency could have resulted in a material misstatement of our annual or interim consolidated financial statements that would not be prevented or detected on a timely basis.
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Previously Disclosed Material Weakness in Internal Controls over Financial Reporting – Consolidated Financial Statement Close Process

As previously disclosed, management identified during the preparation of our audited consolidated financial statements for the year ended June 30, 2023 a material weakness in our internal controls over financial which remains unremediated as of December 31, 2023.

We did not maintain effective internal control over the evaluation and accounting of certain complex and non-routine transactions. Due to an insufficient complement of technical resources within its corporate accounting function, management was unable to complete its evaluation of certain complex non-routine transactions in a timely manner. Specifically, management did not adequately prepare and maintain sufficient evidence of management’s review of (i) significant assumptions, relating to the interim goodwill and long-lived assets impairment assessments as of March 31, 2023, (ii) the evaluation of indicators and assessment of impairment of goodwill and long-lived assets as of June 30, 2023 and (iii) the evaluation of the accounting, measurement and disclosure of events occurring subsequent to the balance sheet date, specifically management’s evaluation of disclosure and the related measurement of a goodwill impairment charge disclosed in the subsequent events footnote.

Previously Disclosed Material Weakness in Internal Control over Financial Reporting – Inventory Reconciliation

As previously disclosed, management identified during the preparation of our audited consolidated financial statements for the year ended June 30, 2023 a material weakness in our internal controls over financial which remains unremediated as of December 31, 2023.

We did not maintain effective internal controls over inventory reconciliation at our Baltimore, Maryland facility. Specifically, we did not implement and design controls at an appropriate level of precision to (i) properly recognize certain third party costs on the balance sheet separately from the inventory balance, (ii) properly and timely update our perpetual inventory subledger to value inventory at lower of cost or market, and (iii) reconcile our perpetual inventory subledger to the related general ledger accounts.

Plan to Remediate Material Weakness in Internal Controls Over Financial Reporting Contract Modifications

The Company, with oversight by the Audit Committee of the Board of Directors of the Company, is devoting significant time, attention, and resources to remediating the contract modification material weakness in our internal controls over financial reporting described above. We have initiated the following steps intended to remediate this material weakness and strengthen our internal controls over financial reporting:

We hired additional technical accounting resources within the corporate controllership group.
Ensuring that appropriate levels of our management, including our necessary technical accounting resources, are consulted before significant contract modifications are executed.

Plan to Remediate Material Weakness in Internal Controls Over Financial Reporting Income Tax Provision

Management, with the oversight of the Audit Committee of the Board, will update our design of controls over the completeness and accuracy of inputs to the quarterly income tax provision calculations.

Plan to Remediate Material Weakness in Internal Controls Over Financial Reporting Revenue Recognition

The Company, with oversight by the Audit Committee of the Board of Directors of the Company, is devoting significant time, attention, and resources to remediating the revenue modification material weakness in our internal controls over financial reporting described above. We are taking initiated the following steps intended to remediate this material weakness and strengthen our internal controls over financial reporting:

We hired additional technical accounting resources within our Bloomington, Indiana site and within the corporate controllership group.
Enhanced the design of our management review controls relating to the accounting for contract modifications, including offered concessions.
Continue to provide additional training for our executive leadership team, and other critical customer-facing personnel, on revenue recognition principles, including contract modifications relating to offered concessions.
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We plan to continue to devote significant time and attention to remediate this material weakness as soon as reasonably practicable. We believe these actions will be sufficient to remediate the identified material weakness and strengthen our internal controls over financial reporting; however, there can be no guarantee that such remediation will be sufficient. We will continue to monitor the design and effectiveness of these and other processes, procedures, and controls and make any further change management determines appropriate. We expect to complete the remediation of this material weakness by the fourth quarter of fiscal 2024, although no assurance can be given regarding the time and effort needed to complete the remediation.

Plan to Remediate Material Weakness in Internal Controls over Financial Reporting – Consolidated Financial Statement Close Process

The Company, with oversight by the Audit Committee of the Board of Directors of the Company, developed and implemented a comprehensive remediation plan which includes the following key initiatives:

we engaged temporary third-party resources with the appropriate level of technical knowledge and experience in accounting related to complex non-routine transactions and the related internal control activities to complement the existing corporate accounting resources;
we continue to hire, develop and retain incremental full-time personnel with appropriate accounting and internal controls expertise;
we will review and update (as appropriate) our methodologies, policies and procedures designed to ensure we are able to more timely address our evaluation of complex non-routine transactions, including the related evidence of management’s review of the significant assumptions used in those evaluations; and
review and update (as appropriate) our training programs related to the relevant internal control over financial reporting matters pertaining to complex non-routine transactions.

We plan to continue to devote significant time and attention to remediate this material weakness as soon as reasonably practicable. We believe these actions will be sufficient to remediate the identified material weakness and strengthen our internal controls over financial reporting; however, there can be no guarantee that such remediation will be sufficient. We will continue to monitor the design and effectiveness of these and other processes, procedures, and controls and make any further change management determines appropriate. We expect to complete the remediation of this material weakness by the fourth quarter of fiscal 2024, although no assurance can be given regarding the time and effort needed to complete the remediation.

Plan to Remediate Material Weakness in Internal Controls Over Financial Reporting Inventory Reconciliation

Management, with oversight by the Audit Committee of the Board, has updated our design of controls for the valuation of inventory at our Baltimore location and we will continue to review and update our procedures as well as provide additional training to the control owners. We believe these actions will be sufficient to remediate the identified material weakness and strengthen our internal controls over financial reporting; however, there can be no guarantee that such remediation will be sufficient. We will continue to monitor the design and effectiveness of these and other processes, procedures, and controls and make any further change management determines appropriate. We expect to complete the remediation of this material weakness by the fourth quarter of fiscal 2024, although no assurance can be given regarding the time and effort needed to complete the remediation.

Changes in Internal Control over Financial Reporting
There
We are taking actions to complete the remediation of the remaining material weaknesses relating to our internal control over financial reporting, as described above. Except as otherwise described herein, there was no change in our internal control over financial reporting (as such term is defined in Rules 13a-15(f) and 15d-15(f) under the Exchange Act) that occurred during our most recent fiscal quarter that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.

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PART II.    OTHER INFORMATION
Item 1.LEGAL PROCEEDINGS
The Company continuesITEM 1.    LEGAL PROCEEDINGS

Information pertaining to receivelegal proceedings can be found in Note 14, Commitments and resolve claims stemming from a prior, temporary, regulatory suspension of one of our manufacturing facilities. To date, more than 30 customers of the facility have presented claims against the Company for alleged losses, including lost profits and other types of indirect or consequential damages that they have allegedly suffered dueContingencies, to the temporary suspension, or have reserved their right to do so subsequently. The CompanyConsolidated Financial Statements and is unable to estimate at this time either the total value of claims that are reasonably possible to be asserted with respect to this matter or the likely cost to resolve them, although (a) as of the end of December 31, 2017, the Company has settled 18 customer claims and (b) certain remaining customers have presented the Company with support for other claims having an aggregate claim value of approximately $4 million. To date, none of the asserted claims takes into account limitations of liability in the contracts governing these claims or any other defense that the Company may assert. In addition, the Company may have insurance for additional costs it may incur as a result of such claims, subject to various deductibles and other limitations, but there can be no assurance as to the aggregate amount or timing of insurance recoveries against any such costs.incorporated by reference herein.
From time to time, the Company may be involved in legal proceedings arising in the ordinary course of business, including, without limitation, inquiries and claims concerning environmental contamination as well as litigation and allegations in connection with acquisitions, product liability, manufacturing or packaging defects and claims for reimbursement for the cost of lost or damaged active pharmaceutical ingredients, the cost of any of which could be significant. The Company intends to vigorously defend itself against any such litigation and does not currently believe that the outcome of any such litigation will have a material adverse effect on the Company’s financial statements. In addition, the healthcare industry is highly regulated and government agencies continue to scrutinize certain practices affecting government programs and otherwise.
From time to time, the Company receives subpoenas or requests for information relating to the business practices and activities of customers or suppliers from various governmental agencies or private parties, including from state attorneys general, the U.S. Department of Justice, and private parties engaged in patent infringement, antitrust, tort, and other litigation. The Company generally responds to such subpoenas and requests in a timely and thorough manner, which responses sometimes require considerable time and effort and can result in considerable costs being incurred. The Company expects to incur costs in future periods in connection with future requests.
Item 1A.RISK FACTORS
ITEM 1A.    RISK FACTORS
In addition to the other information set forth in this report,Quarterly Report on Form 10-Q, you should carefully consider the factors discussed in the section entitled “Risk Factors” in our Annual Report on FormFiscal 2023 10-K, for the fiscal year ended June 30, 2017, which could materially affect our business, financial condition, or future results. The risks described in our Annual Report on FormFiscal 2023 10-K are not the only risks facing us. Additional risks and uncertainties not currently known to us or that we currently deem to be immaterial also may materially adversely affect our business, financial condition, and/or operating results.

We may not complete the pending Merger with Novo Holdings within the timeframe anticipated, or at all, which could have a material adverse effect on our business, financial condition or results of operations, as well as negatively impact our share price.

On February 5, 2024, we entered into an Agreement and Plan of Merger (the “Merger Agreement”) with Creek Parent, Inc. (“Parent”), a Delaware corporation and a wholly owned subsidiary of Novo Holdings A/S (“Novo Holdings”), and Creek Merger Sub, Inc., a Delaware corporation and a wholly owned subsidiary of Parent (“Merger Sub”). The Merger Agreement provides that, upon the terms and subject to the conditions set forth therein and in accordance with the General Corporation Law of the State of Delaware, Merger Sub will be merged with and into the Company, with the Company surviving the Merger as a wholly owned subsidiary of Parent (the “Merger”).

Consummation of the Merger is subject to customary closing conditions, including (i) approval of the Merger by the Company’s stockholders, (ii) receipt of certain governmental waivers, consents, clearances, decisions, declarations, approvals, and expirations of applicable waiting periods, including the expiration or early termination of the waiting period under the U.S. Hart-Scott-Rodino Antitrust Improvements Act of 1976, with respect to (A) the Merger and (B) the sale of three of the Company’s fill-finish sites (which are located in Anagni, Italy, Bloomington, Indiana USA, and Brussels, Belgium) and related assets from Novo Holdings to Novo Nordisk A/S, of which Novo Holdings has a controlling interest (the “Carve-Out”), (iii) the absence of any order, injunction or law prohibiting the Merger or the Carve-Out, in each case, without a Burdensome Condition (as defined in the Merger Agreement), and (iv) the absence of a Material Adverse Effect (as defined in the Merger Agreement) on the Company. Furthermore, the granting of regulatory approvals by antitrust authorities could involve the imposition of additional conditions on the closing of the Merger. The imposition of such conditions or the failure or delay to obtain regulatory approvals could have the effect of delaying completion of the Merger or of imposing additional costs or limitations on us or may result in the failure to close the Merger. We cannot provide any assurance that the conditions to the consummation of the Merger will be satisfied or waived or that, if the Merger is consummated, it will be on the terms specified in the Merger Agreement or within the anticipated timeframe.

Failure to complete the Merger within the timeframe anticipated could adversely affect our business and the market price of our Shares in a number of ways, including:

The price of our common stock may decline to the extent that current market prices of our common stock reflect assumptions that the Merger will be completed on a timely basis.

We could be required to pay Novo Holdings a termination fee of approximately $345 million if the Merger Agreement is terminated under specific circumstances described in the Merger Agreement.

The failure to complete the Merger may result in negative publicity and negatively affect our relationship with our stockholders, employees, customers, suppliers and lenders.

If the Merger is not completed, the time and resources committed by our management team could have been devoted to pursuing other opportunities.

We have incurred, and will continue to incur, significant expenses for professional services in connection with the Merger for which we will have received little or no benefit if the Merger is not completed.

In addition, any litigation or enforcement proceeding commenced against us in connection with the Merger may require us to devote significant time and resources and could require us to incur significant costs. This also could result in the Merger being delayed and/or enjoined by a court of competent jurisdiction, which could prevent the Merger from becoming effective.
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The occurrence of any of these events individually or in combination which could have a material adverse effect on our business, financial condition or results of operations, as well as negatively impact our share price.

The announcement and pendency of the Merger with Novo Holdings could materially adversely affect our business, financial condition or results of operations, as well as negatively impact our share price.

Our efforts to complete the Merger with Novo Holdings could cause substantial disruptions in, and create uncertainty surrounding, our business, which may materially adversely affect our business, financial condition or results of operations, or the price of our common stock. Uncertainty as to whether the Merger will be completed may affect our ability to recruit prospective employees or to retain and motivate existing employees. Employee retention may be particularly challenging while the transaction is pending because employees may experience uncertainty about their roles following consummation of the Merger. A substantial amount of our management’s and employees’ attention is being directed toward the completion of the transaction and thus is being diverted from our day-to-day operations. Uncertainty as to our future also could adversely affect our business and our relationship with collaborators, strategic partners, suppliers, existing or prospective customers or regulators. For example, collaborators, suppliers, existing or prospective customers and other counterparties may defer decisions concerning us, or seek to change existing business relationships with us, whether pursuant to the terms of their existing agreements with us or otherwise. Changes to or termination of existing business relationships could materially adversely affect our financial condition and results of operations, as well as negatively impact our share price. The adverse effects of the pendency of the transaction could be exacerbated by any delays in completion of the transaction, changes to the terms of the transaction or termination of the Merger Agreement.

In certain instances, the Merger Agreement requires us to pay a termination fee to Novo Holdings, which could require us to use available cash that would have otherwise been available for general corporate purposes and other uses.

The Merger Agreement contains certain termination rights for us and Novo Holdings. Subject to certain limitations, we or Novo Holdings may terminate the Merger Agreement if the Merger is not closed by February 5, 2025 (as may be extended as described in the following sentence, the “End Date”), either the Company or Parent may terminate the Merger Agreement. However, if as of such End Date all conditions set forth in the Merger Agreement have been satisfied or waived (other than those conditions that (i) by their nature are to be satisfied by actions to be taken at the closing, or (ii) relate to receipt of required regulatory approvals or legal restraints in connection with required regulatory approvals or applicable antitrust laws), then the End Date will automatically be extended by three (3) months on each of four (4) occasions. In addition, if the condition relating to receipt of the Company’s stockholders’ approval has not been satisfied solely due to the Company’s inability to timely file the Merger proxy statement in certain limited circumstances, then, subject to the satisfaction or waiver of all conditions other than the foregoing and those noted in the preceding sentence, the End Date will be extended by three (3) months on each of the first two (2) such occasions.

Upon termination of the Merger Agreement, the Company, under specified circumstances and conditions set forth in the Merger Agreement, including termination (1) by the Company in order to enter into an alternative acquisition agreement with respect to a Superior Offer (as defined in the Merger Agreement) or (2) by Parent upon a change in our board of directors’ stockholder recommendation of the Merger, will be required to pay Parent a termination fee equal to $345 million.

If the Merger Agreement is terminated under such circumstances, the termination fee we would be required to pay under the Merger Agreement may require us to use available cash that would have otherwise been available for general corporate purposes and other uses. Further, a failed transaction may result in negative publicity and a negative impression of us in the investment community. For these and other reasons, termination of the Merger Agreement could materially and adversely affect our business, results of operations and financial condition, which in turn would materially and adversely affect the price of our common stock.

We have incurred, and will continue to incur, direct and indirect costs as a result of the pending Merger with Novo Holdings.

We have incurred, and will continue to incur, significant costs and expenses, including legal, accounting and other advisory fees and other transaction costs, in connection with the pending Merger. We will be required to pay a substantial portion of these costs and expenses whether or not the Merger is completed. There are a number of factors beyond our control that could affect the total amount or the timing of these costs and expenses.

While the Merger Agreement is in effect, we are subject to restrictions on our business activities.

While the Merger Agreement is in effect, we are subject to restrictions on our business activities, generally requiring us to conduct our business in the ordinary course, consistent with past practice, in all material respects, and subjecting us to a variety of specified limitations absent Novo Holdings’ prior consent. These limitations include, among other things, restrictions on our ability to acquire other businesses and material assets (including certain governmental licenses and authorizations), dispose of material assets, make investments, enter into or amend certain material contracts, repurchase or issue securities, pay dividends,
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make capital expenditures, take certain actions relating to intellectual property, amend our organizational documents, incur indebtedness, hire/terminate certain employees and provide increases to compensation and benefits to certain employees. These restrictions could prevent us from pursuing strategic business opportunities, taking actions with respect to our business that we may consider advantageous and responding effectively or on a timely basis to competitive pressures and industry developments, and may as a result materially adversely affect our business, financial condition and results of operations.

The Merger Agreement contains provisions that could deter or make it difficult for a third party from proposing an alternative transaction or acquire our Company prior to the consummation of the Merger.

The Merger Agreement contains provisions that limit our ability to entertain a third-party proposal for an acquisition of our company or an alternative transaction in lieu of the Merger. These provisions include our agreement not to, directly or indirectly, solicit, initiate, or knowingly facilitate, or knowingly encourage or negotiate with any person regarding other proposals for an acquisition of our Company, as well as restrictions on our ability to respond to such proposals, subject to certain exceptions including fulfillment of certain fiduciary requirements of our board of directors. In addition, we could be required to pay Novo Holdings a termination fee of approximately $344.8 million if the Merger Agreement is terminated under specific circumstances. These or other provisions in the Merger Agreement might discourage a third party with a potential interest in acquiring all or a significant part of the outstanding shares of our common stock from considering or proposing an acquisition, even one that may be deemed of greater value to our stockholders than the proposed Merger with Novo Holdings. Furthermore, even if a third party elects to propose an acquisition of us, the potential competing acquirer may propose to pay a lower amount as a result of the termination fee that will become payable by us.

We may be targets of securities class action and derivative lawsuits that could result in substantial costs and may delay or prevent the Merger from being completed.

Securities class action lawsuits and derivative lawsuits are often brought against public companies that have entered into merger agreements. The outcome of litigation is uncertain and we may not be successful in defending against future claims brought against us even if they are without merit. Regardless of the outcome of any lawsuits brought against us, such lawsuits could delay or prevent the Merger, divert the attention of our management and employees from our day-to-day business, result in substantial costs and otherwise adversely affect us financially. A potential adverse judgment could result in monetary damages, which could have a negative impact on our liquidity and financial condition. Additionally, if a plaintiff is successful in obtaining an injunction prohibiting completion of the Merger, that injunction may delay or prevent the Merger from being completed, or from being completed within the anticipated timeframe, which may adversely affect our business, financial condition or results of operations.

Our executive officers and directors may have interests in the proposed Merger that are different from, or in addition to, those of our stockholders generally.

Our executive officers and directors may have interests in the proposed Merger that are different from the interests of our stockholders generally, including, among others, the acceleration of the vesting of equity awards and receipt of change in control or other severance payments in connection with the proposed Merger, continued indemnification and insurance and potentially continued service to the combined company. These interests, among others, may influence, or appear to influence, our executive officers and directors and cause them to view the Merger differently from how our stockholders generally may view it.

Additional information regarding our executive officers and directors and their interests in the proposed Merger will be included in the proxy statement relating to the proposed Merger when it is filed with the Securities and Exchange Commission.

If the Merger occurs, our stockholders will not be able to participate in any further upside to our business.

If the Merger is consummated, our stockholders will receive the right to receive an amount in cash equal to $63.50 per Share, without interest, and will not receive any equity interests of Parent. As a result, if our business following the Merger performs well, our current stockholders will not receive any additional consideration and will therefore not receive any benefit from any such future performance of our business.
Other than what was disclosed in the Special Note Regarding Forward-Looking Statements and discussed below,risk factors noted above, there has been no material change to the risk factors disclosed in the Company’s Annual Report on Form 10-K.
The following information amends, updates, and should be read in conjunction with the risk factors and information disclosed in theour Fiscal 20172023 10-K.
The impact to our business of recently enacted U.S. tax legislation could differ materially from our current estimates.
On December 22, 2017, the U.S. government enacted wide-ranging tax legislation, the 2017 Tax Act. The 2017 Tax Act significantly revises U.S. tax law by, among other provisions, lowering the applicable U.S. federal statutory income tax rate from 35% to 21%, creating a partial territorial tax system that includes a mandatory one-time transition tax on previously deferred foreign earnings, and eliminating or reducing certain income tax deductions.
Although we are still determining whether the 2017 Tax Act will ultimately benefit our results of operations and financial condition in future periods, primarily by reducing the applicable U.S. federal statutory income tax rate from 35% to 21%, we recorded a one-time net charge of $46.0 million within our income tax provision as a provisional estimate of the net accounting impact of the 2017 Tax Act in the second quarter of fiscal 2018. We recorded this charge on a provisional basis, based on our present understanding of the 2017 Tax Act and other information available as of the time of the estimates, including assumptions and expectations about future events.
Although we believe these provisional amounts represent a reasonable estimate of the ultimate enactment-related impact the 2017 Tax Act will have on our consolidated financial statements, we may adjust these amounts materially as additional information becomes available and we complete further analyses. The impact of the 2017 Tax Act to our business in future

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periods is also subject to a variety of factors beyond our control including, but not limited to, (i) potential amendments to the 2017 Tax Act; (ii) potential changes to state, local, and foreign tax laws in response to the 2017 Tax Act; and (iii) potential new or interpretative guidance issued by the SEC, the Financial Accounting Standards Board or the Internal Revenue Service related to the 2017 Tax Act. Any of these factors could cause our actual results to differ materiality from our current expectations and/or investors’ expectations. Further, there are certain effects of the 2017 Tax Act we cannot reasonably estimate, including (a) the GILTI rules, (b) the FDII deduction, (c) the BEAT, (d) provisions eliminating or reducing certain income tax deductions, such as interest expense, and certain employee expenses, and (e) the state tax impact of the 2017 Tax Act. As we gather, analyze, and consider additional data in the context of the 2017 Tax Act and ASC 740 Income Taxes, we may adjust in future periods our current estimates, but we will do so only during the measurement period prescribed by SAB 118. Any such adjustment may be material.
Item 2.
ITEM 2.    UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
None.


PurchaseRecent Sales of Unregistered Equity Securities

We did not sell any unregistered equity securities during the period covered by this Quarterly Report.
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Issuer Purchases of Equity Securities
None.
We did not purchase any of our equity securities during the period covered by this Quarterly Report.

Item 3.DEFAULTS UPON SENIOR SECURITIES
ITEM 3.    DEFAULTS UPON SENIOR SECURITIES

None.

Item 4.MINE SAFETY DISCLOSURES
ITEM 4.    MINE SAFETY DISCLOSURES

Not applicable.

ITEM 5.    OTHER INFORMATION

Trading Arrangements

During the fiscal quarter ended December 31, 2023, our directors and officers (as defined in Rule 16a-1(f) under the Exchange Act) adopted or terminated the contracts, instructions or written plans for the purchase or sale of our securities as set forth in the table below:
Item 5.
Trading ArrangementOTHER INFORMATION
Name and TitleActionDateRule10b5-1*Non-Rule 10b5-1**Total Shares of Common Stock to be SoldExpiration Date
Scott Gunther, Senior Vice President of Quality & Regulatory AffairsAdoptDecember 14, 2023X
Up to 1650 shares(1)
August 5, 2024(2)

Not applicable.* Intended to satisfy the affirmative defense of Rule 10b5-1(c)

** “Non-Rule 10b5-1 trading arrangement” as defined in Item 408(c) of Regulation S-K under the Exchange Act.

(1) Represents up to 50% of the shares (i) scheduled to vest under two option awards granted to the officer (after the sale of shares to cover any applicable taxes) and (ii) previously issued to the officer upon achievement of the fiscal 2021-23 performance-based vesting criteria.

(2) Trading plan will terminate on the earlier to occur of (a) August 5, 2024; (b) the execution of all trades or expiration of all of the orders relating to such trades; (c) the date the broker receives notice of liquidation, dissolution, bankruptcy, insolvency, or death of the officer; (d) the date the broker receives notice from the officer or officer’s agent of his termination of the trading plan; (e) the date the broker determines, in its sole discretion, that the trading plan has been terminated, including, without limitation, where the broker determines there has been a modification or change to the trading plan that constitutes the termination of the trading plan; (f) the date the broker notifies the officer of the broker’s termination of the trading plan due to the officer’s breach of any of the terms of the trading plan or in the event that the officer trades shares outside of the trading plan; or (g) the date the broker exercises any other termination right it may have under the trading plan.

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ItemITEM 6.    EXHIBITS
Exhibits:
Agreement and Plan of Merger, dated as of February 5, 2024, by and among the Company, Creek Parent, Inc., and Creek Merger Sub, Inc. (incorporated by reference to Exhibit 2.1 to the Current Report on Form 8-K filed on February 5, 2024).
Offer letter,Amendment No. 10 to Amended and Restated Credit Agreement, dated January 31, 2018, between Wetteny Josephas of November 22, 2023, by and among Catalent Pharma Solutions, Inc., PTS Intermediate Holdings LLC, JPMorgan Chase Bank, N.A., as the administrative agent, collateral agent, swing line lender, and letter of credit issuer, and the lenders and other parties thereto, which amends that certain Amended and Restated Credit Agreement, dated as of May 20, 2014 (as amended), by and among Catalent Pharma Solutions, Inc., PTS Intermediate Holdings LLC, JPMorgan Chase Bank, N.A., as the successor administrative agent, collateral agent, swing line lender, and letter of credit issuer, and the lenders and other parties thereto (incorporated by reference to Exhibit 10.1 to the Company's current reportCurrent Report on Form 8-K filed on February 5, 2018, File No. 001-36587) †November 27, 2023).
Amendment No. 11 to Amended and Restated Credit Agreement, dated as of December 19, 2023, by and among Catalent Pharma Solutions, Inc., PTS Intermediate Holdings LLC, JPMorgan Chase Bank, N.A., as the administrative agent, collateral agent, swing line lender, and letter of credit issuer, and the lenders and other parties thereto, which amends that certain Amended and Restated Credit Agreement, dated as of May 20, 2014 (as amended), by and among Catalent Pharma Solutions, Inc., PTS Intermediate Holdings LLC, JPMorgan Chase Bank, N.A., as the successor administrative agent, collateral agent, swing line lender, and letter of credit issuer, and the lenders and other parties thereto (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed December 19, 2023).
Termination Agreement, dated as of December 28, 2023, by and between Catalent Pharma Solutions GmbH and Manja Boerman. †*
Amendment No.1 to Catalent, Inc. 2018 Omnibus Incentive Plan (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on January 26, 2024). †
Certification of the Chief Executive Officer pursuant to Rule 13a-14(a) or Rule 15d-14(a) of the Securities Exchange Act of 1934, as amended*amended. *
Certification of the Chief Financial Officer pursuant to Rule 13a-14(a) or Rule 15d-14(a) of the Securities Exchange Act of 1934, as amended*amended. *
Certification of the Chief Executive Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002**2002. **
Certification of the Chief Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002**2002. **
101.1101The following financial information from Catalent, Inc.’s Quarterly Report on Form 10-Q for the quarter ended December 31, 20172023 formatted in inline XBRL: (i) Consolidated Statements of Operations for the Three and NineSix Months Ended December 31, 20172023 and 2016;2022; (ii) Consolidated Statements of Comprehensive Income/(Loss)Loss for the Three and NineSix Months Ended December 31, 20172023 and 20162022 (iii) Consolidated Balance Sheets as of December 31, 20172023 and June 30, 2017;2023; (iv) Consolidated Statement of Changes in Shareholders’ Equity/(Deficit) as ofEquity for the Three and Six Months Ended December 31, 2017;2023 and 2022; (v) Consolidated Statements of Cash Flows for the Six Months Ended December 31, 20172023 and 2016;2022; and (vi) Notes to Unaudited Consolidated Financial Statements.
104The cover page of this Quarterly Report on Form 10-Q, formatted as Inline XBRL and contained in Exhibit 101.
*Filed herewith
**Furnished herewith
Represents a management contract, compensatory plan or arrangement in which directors and/or executive officers are eligible to participate.
* Filed herewith
** Furnished herewith
† Represents a management contract, compensatory plan or arrangement in which the directors and/or executive officers are eligible to participate.

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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

CATALENT, INC.
(Registrant)
Date:February 14, 2024By:/s/ MATTI MASANOVICH
Date:February 5, 2018By:/s/ John R. ChiminskiMatti Masanovich
John R. Chiminski
President & Chief Executive Officer
Date:February 5, 2018By:/s/ Matthew M. Walsh
Matthew M. Walsh
ExecutiveSenior Vice President &and Chief Financial Officer


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