Table of Contents

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
 ______________________________
FORM 10-Q
______________________________ 
ýQUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended December 31, 20202021
or
¨TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
001-36587
(Commission File Number)
ctlt-20211231_g1.jpg
 _____________________________
Catalent, Inc.
(Exact name of registrant as specified in its charter)
_____________________________ 
Delaware 20-8737688
(State or other jurisdiction of incorporation or organization) (I.R.S. Employer Identification No.)
14 Schoolhouse Road,SomersetNJ 08873
(Address of principal executive offices) (Zip code)
(732) 537-6200
Registrant's telephone number, including area code
__________________________________________________________________ 
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 ¨  No
Indicate by check mark whether the registrant has submitted electronically 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 such files).       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 filerAccelerated filer¨
Non-accelerated filer¨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 

Securities registered pursuant to Section 12(b) of the Act:
Title of each classTrading symbols(s)Name of each exchange on which registered
Common StockCTLTNew York Stock Exchange

On January 25, 2021,2022, there were 170,226,514179,104,173 shares of the Registrant's common stock, par value $0.01 per share, issued and outstanding.



Table of Contents
CATALENT, INC. and Subsidiaries
Index to Form 10-Q
For the Three and Six Months Ended December 31, 20202021
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 contain “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, 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 described under the section entitled “Risk Factors” in our Annual Report on Form 10-K for the fiscal year ended June 30, 20202021 (the “Fiscal 20202021 10-K”) and others, which are summarized below:
Risks Relating to Our Business and the following:Industry in Which We Operate

Our business, financial condition, and results of operations may be adversely affected by global health epidemics,developments, including the novelpandemic resulting from the SARS-Co-V-2 strain of coronavirus and its variants (“COVID-19”) pandemic..
The continually evolving nature of the COVID-19 pandemic and the resulting public health response, including the changing demand for various COVID-19 vaccines and treatments from both patients and governments around the world, may affect sales of our products and services, including the COVID-19 products we manufacture.
We participate in a highly competitive market, and increased competition may adversely affect our business.
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. In addition, customer spending may be affected by, among other things, the COVID-19 pandemic or recessionary economic conditions caused in whole or in part by the pandemic.
We are subject to product and other liability risks that could exceed our anticipated costs or adversely affect our results of operations, financial condition, liquidity, and cash flows.
FailureWe are a part of the highly regulated healthcare industry, subject to complystringent regulatory standards and other applicable laws and regulations, which can change unexpectedly and may adversely impact our business.
Any failure to implement fully, monitor, and improve our quality management strategy could lead to quality or safety issues and expose us to significant costs, potential liability, and adverse publicity.
If we cannot keep pace with existingrapid technological advances, our services may become uncompetitive or obsolete.
Any failure to protect or maintain our intellectual property may adversely affect our competitive edge and future regulatory requirements could adversely affectresult in loss of revenue and reputation.
Future price fluctuations, material shortages of raw materials, or changes in healthcare policies may have an adverse effect on our results of operations and financial condition or result in claims from customers.conditions.
FailureOur ability to provide quality offerings touse our customers could have an adverse effect on our businessnet operating loss carryforwards and subject us to regulatory actions or costly litigation.certain other tax attributes may be limited.
The servicesWe may be unable to attract or retain key personnel.
We may be unsuccessful in integrating our acquisitions, and offerings we provide are highly exactingmay expend substantial amounts of cash and complex, and, if we encounter problems providing the services or support required, our business could suffer.incur debt in making acquisitions.
Our global operations are subject to economic and political and regulatory risks, including the risks of changing regulatory standards or changing interpretations of existing standards, thatwhich could affect the profitability of our operations or require costly changes to our procedures. In addition, changes to our procedures, or additional procedures, implemented to comply with public health orders or best practice guidelines as a result of the COVID-19 pandemic may increase our costs or reduce our productivity and thereby affect our business, financial condition, or results of operations.
The exit of the United Kingdom (the “U.K.”) from the European Union could have future adverse effects on our operations, 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 or buy less of them, and our revenue and profitability may decline.
We and our customers depend on patents, copyrights, trademarks, know-how, trade secrets, and other forms of intellectual property protections, but these protections may not be adequate.
Our offering or our customers’ products may infringe on the intellectual property rights of third parties.
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. In addition, the COVID-19 pandemic may interfere with the
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operations of certain of our direct or indirect suppliers or with international trade for these supplies, which may either raise our costs or reduce the productivity or slow the timing of our operations.
Changes in market access or healthcare reimbursement for our customers’ products in the United States (“U.S.”) or other countries, including possible changes to the U.S. Affordable Care Act, could adversely affect our results of operations and financial condition by affecting demand for our offerings or the financial health of our customers.
As a global enterprise, fluctuations in the exchange rate of the United States ("U.S.") dollar, our reporting currency, against other currencies could have a material adverse effect on our financial performance and results of operations.
Tax legislative or regulatory initiatives, new interpretations or developments concerning existing tax laws, or challenges to our tax positions could adversely affect our results of operations and financial condition.
Our ability to use our net operating loss carryforwards, foreign tax credit carryforwards, and certain other tax attributes may be limited.
Changes to the estimated future profitability of the business may require that we establish an additional valuation allowance against all or some portion of our net deferred tax assets.
We depend on key personnel whose continued employment and engagement at current levels cannot be assured.
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, and the risks generally associated with information and communications systems could adversely affect our results of operations. We are
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continuously working to install new, and upgrade existing, systems and provide employee awareness training around phishing, malware, and other cyber-securitycyber security risks to enhance the protections available to us, but such protections may be inadequate to address malicious attacks or inadvertent compromises of data security.
We engage from time to time in acquisitions 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 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 full benefits from any such transaction could have a negative effect on our operations.
Cell and gene therapies are relatively new and still-developing modes of treatment dependent on cutting-edge technologies, and our customers’ cell or gene therapies may be perceived as unsafe or may result in unforeseen adverse events. Negativesubject to changing public opinion, continuing research, orand increased regulatory scrutiny, each of cell or gene therapies and their financial costwhich may damage public perception of the safety, utility, or efficacy of cell or gene therapies and harmaffect our customers’customers' ability to conduct their business, or obtain regulatory approvals for their cell or gene therapy products,therapies, and thereby have an indirect, adverse effect onadversely affect our cell or gene therapy offerings.

We are subject
Risks Relating to environmental, health, and safety laws and regulations, which could increase our costs and restrict our operations in the future.Our Indebtedness
We are subject to labor and employment laws and regulations, which could increase our costs and restrict our operations in the future.
Certain of our pension plans are underfunded, 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 leverage could adversely affect our ability to raise additional capital to fund our operations, limit our ability to reactoperate our business and to changes in the economyfinance future operations or inacquisitions that would enhance our industry, expose us to interest-rate risk to the extent of our variable rate debt, and 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.growth.
Our debt agreements contain restrictions that may limit our flexibility in operating our business.
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Despite the limitations in our debt agreements, we retain the ability to takeconducting certain actions that may interfere with our ability timely to pay our substantial indebtedness.current and future operations.
We are currently usingmay not be able to pay our indebtedness when it becomes due.
Our current and may in thepotential future use of 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 relatedeconomic losses in the event of price or currency fluctuations.

Risks Relating to counterparty credit worthinessOwnership of Our Common Stock

Our stock price has historically been and may continue to be volatile.
Because we have no plan to pay cash dividends on our common stock, par value $0.01 (the “Common Stock”) for the foreseeable future, receiving a return on an investment in our Common Stock may require a sale for a net price greater than was paid for it.
Provisions in our organizational documents could delay or non-performanceprevent a change of these instruments.control.

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), and our corporate Twitter account (@catalentpharma) as channels for the distribution of information. 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”) filings, and public conference calls and webcasts. The contents of our website and social media channels are not, however, a part of this report.
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PART I.    FINANCIAL INFORMATION

ItemITEM 1.     FINANCIAL STATEMENTS

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


Three Months Ended  
December 31,
Six Months Ended  
December 31,
2020201920202019
Net revenue$910.8 $721.4 $1,756.5 $1,386.1 
Cost of sales612.6 489.2 1,209.4 976.2 
Gross margin298.2 232.2 547.1 409.9 
Selling, general, and administrative expenses165.5 141.0 330.2 283.8 
Impairment charges and (gain) loss on sale of assets0.6 1.7 2.4 1.5 
Restructuring and other5.5 0.5 6.4 1.2 
Operating earnings126.6 89.0 208.1 123.4 
Interest expense, net25.9 34.9 51.2 71.2 
Other (income) expense, net(8.3)(4.4)(19.5)0.5 
Earnings before income taxes109.0 58.5 176.4 51.7 
Income tax expense20.6 13.0 5.6 6.1 
Net earnings88.4 45.5 170.8 45.6 
Less: Net earnings attributable to preferred shareholders(11.8)(11.2)(25.4)(18.7)
Net earnings attributable to common shareholders$76.6 $34.3 $145.4 $26.9 
Earnings per share:
Basic
Net earnings$0.46 $0.23 $0.88 $0.18 
Diluted
Net earnings$0.45 $0.23 $0.87 $0.18 

Three Months Ended  
December 31,
Six Months Ended  
December 31,
2021202020212020
Net revenue$1,217 $911 $2,242 $1,757 
Cost of sales812 613 1,513 1,210 
Gross margin405 298 729 547 
Selling, general, and administrative expenses228 165 411 330 
Gain on sale of subsidiary— — (1)— 
Other operating expense16 20 
Operating earnings161 127 299 208 
Interest expense, net32 26 58 51 
Other expense (income), net14 (8)23 (19)
Earnings before income taxes115 109 218 176 
Income tax expense18 21 28 
Net earnings97 88 190 171 
Less: Net earnings attributable to preferred shareholders(4)(11)(13)(26)
Net earnings attributable to common shareholders$93 $77 $177 $145 
Earnings per share:
Basic
Net earnings$0.53 $0.46 $1.02 $0.88 
Diluted
Net earnings$0.52 $0.45 $1.01 $0.87 










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
(Unaudited; dollars in millions)


Three Months Ended  
December 31,
Six Months Ended  
December 31,
2020201920202019
Net earnings$88.4 $45.5 $170.8 $45.6 
Other comprehensive income, net of tax
Foreign currency translation adjustments39.4 22.1 55.3 0.3 
Pension and other post-retirement adjustments0.5 3.3 1.0 3.0 
Derivatives and hedges0.5 0.4 
Other comprehensive income, net of tax40.4 25.4 56.7 3.3 
Comprehensive income$128.8 $70.9 $227.5 $48.9 

Three Months Ended  
December 31,
Six Months Ended  
December 31,
2021202020212020
Net earnings$97 $88 $190 $171 
Other comprehensive (loss) income, net of tax
Foreign currency translation adjustments(18)39 (32)55 
Pension and other post-retirement adjustments— 
Net change in marketable securities(1)— (1)— 
Derivatives and hedges— 
Other comprehensive (loss) income, net of tax(16)40 (28)57 
Comprehensive income$81 $128 $162 $228 






















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; in millions, except share and per share data)
December 31,
2020
June 30,
2020
ASSETS
Current assets:
Cash and cash equivalents$833.1 $953.2 
Trade receivables, net771.5 838.1 
Inventories461.3 323.8 
Prepaid expenses and other453.0 177.9 
Total current assets2,518.9 2,293.0 
Property, plant, and equipment, net2,129.8 1,900.8 
Other assets:
Goodwill2,461.5 2,470.6 
Other intangibles, net855.3 888.7 
Deferred income taxes44.6 49.4 
Other long-term assets188.0 174.0 
Total assets$8,198.1 $7,776.5 
LIABILITIES, REDEEMABLE PREFERRED STOCK, AND SHAREHOLDERS' EQUITY
Current liabilities:
Current portion of long-term obligations and other short-term borrowings$72.0 $72.9 
Accounts payable356.9 321.0 
Other accrued liabilities595.1 499.3 
Total current liabilities1,024.0 893.2 
Long-term obligations, less current portion2,983.8 2,945.1 
Pension liability141.9 135.2 
Deferred income taxes66.5 94.0 
Other liabilities167.4 203.6 
Commitment and contingencies (see Note 14)
Total liabilities4,383.6 4,271.1 
Redeemable preferred stock, $0.01 par value; 1.0 million shares authorized at December 31 and June 30, 2020; 384,777 and 650,000 shares issued and outstanding at December 31 and June 30, 2020, respectively359.0 606.6 
Shareholders' equity:
Common stock, $0.01 par value; 1.0 billion shares authorized at December 31 and June 30, 2020; 170.1 million and 162.8 million issued and outstanding at December 31 and June 30, 2020, respectively1.7 1.6 
Preferred stock, $0.01 par value; 99 million authorized at December 31 and June 30, 2020; 0 issued and outstanding at December 31 and June 30, 2020
Additional paid in capital4,160.8 3,818.7 
Accumulated deficit(377.4)(535.2)
Accumulated other comprehensive loss(329.6)(386.3)
Total shareholders' equity3,455.5 2,898.8 
Total liabilities, redeemable preferred stock, and shareholders' equity$8,198.1 $7,776.5 


December 31,
2021
June 30,
2021
ASSETS
Current assets:
Cash and cash equivalents$849 $896 
Trade receivables, net of allowance for credit losses of $23 and $12, respectively871 1,012 
Inventories688 563 
Prepaid expenses and other500 376 
Marketable securities66 71 
Total current assets2,974 2,918 
Property, plant, and equipment, net of accumulated depreciation of $1,255 and $1,179, respectively2,727 2,524 
Other assets:
Goodwill3,026 2,519 
Other intangibles, net1,132 817 
Deferred income taxes65 66 
Other long-term assets279 268 
Total assets$10,203 $9,112 
LIABILITIES, REDEEMABLE PREFERRED STOCK, AND SHAREHOLDERS' EQUITY
Current liabilities:
Current portion of long-term obligations and other short-term borrowings$29 $75 
Accounts payable363 385 
Other accrued liabilities653 736 
Total current liabilities1,045 1,196 
Long-term obligations, less current portion4,191 3,166 
Pension liability127 137 
Deferred income taxes189 164 
Other liabilities170 175 
Commitment and contingencies (see Note 15)— — 
Total liabilities5,722 4,838 
Redeemable preferred stock, $0.01 par value; 0 and 1 million shares authorized at December 31 and June 30, 2021, respectively; 0 and 0.4 million shares issued and outstanding at December 31 and June 30, 2021, respectively— 359 
Shareholders' equity:
Common stock, $0.01 par value; 1.00 billion shares authorized at December 31 and June 30, 2021; 179 million and 171 million issued and outstanding at December 31 and June 30, 2021, respectively
Preferred stock, $0.01 par value; 100 million shares and 99 million shares authorized at December 31 and June 30, 2021, respectively; 0 shares issued and outstanding at December 31 and June 30, 2021— — 
Additional paid in capital4,615 4,205 
Retained earnings209 25 
Accumulated other comprehensive loss(345)(317)
Total shareholders' equity4,481 3,915 
Total liabilities, redeemable preferred stock, and shareholders' equity$10,203 $9,112 
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
(Unaudited; dollars in millions, except share data in thousands)
 

Three Months Ended December 31, 20202021
Shares of Common StockCommon StockAdditional Paid in CapitalAccumulated DeficitAccumulated Other Comprehensive LossTotal Shareholders' EquityRedeemable Preferred Stock
Balance at September 30, 2020164,567.1 $1.6 $3,901.4 $(460.9)$(370.0)$3,072.1 $606.6 
Share issuances related to
     stock-based compensation
173.9 — — — — 
Conversion of redeemable
preferred stock
5,392.3 0.1 252.9 — — 253.0 (247.6)
Stock-based compensation— — 11.4 — — 11.4 — 
Cash paid, in lieu of equity,
     for tax withholding
— — (6.8)— — (6.8)— 
Employee stock purchase plan— — 1.9 — — 1.9 — 
Preferred dividend ($12.50 per
share of redeemable preferred
stock)
— — — (4.9)— (4.9)— 
Net earnings— — — 88.4 — 88.4 — 
Other comprehensive income, net
of tax
— — — — 40.4 40.4 — 
Balance at December 31, 2020170,133.3 $1.7 $4,160.8 $(377.4)$(329.6)$3,455.5 $359.0 
Shares of Common StockCommon StockAdditional Paid in CapitalRetained EarningsAccumulated Other Comprehensive LossTotal Shareholders' EquityRedeemable Preferred Stock
Balance at September 30, 2021171,033 $2 $4,234 $114 $(329)$4,021 $359 
Share issuances related to stock-
     based compensation
199 — — — — — — 
Conversion of redeemable
     preferred stock
7,818 — 362 — — 362 (359)
Stock-based compensation— — 11 — — 11 — 
Cash paid, in lieu of equity, for
     tax withholding
— — (5)— — (5)— 
Exercise of stock options— — 11 — — 11 — 
Employee stock purchase plan— — — — — 
Preferred dividend ($12.50 per
     share of redeemable preferred
     stock)
— — — (2)— (2)— 
Net earnings— — — 97 — 97 — 
Other comprehensive income, net
of tax
— — — — (16)(16)— 
Balance at December 31, 2021179,050 $2 $4,615 $209 $(345)$4,481 $ 


Three Months Ended December 31, 2019
Shares of Common StockCommon StockAdditional Paid in CapitalAccumulated DeficitAccumulated Other Comprehensive LossTotal Shareholders' EquityRedeemable Preferred Stock
Balance at September 30, 2019146,235.7 $1.5 $2,755.2 $(731.4)$(376.0)$1,649.3 $606.6 
Share issuances related to stock-
     based compensation
123.8 — — — 
Stock-based compensation— — 10.3 — — 10.3 
Cash paid, in lieu of equity, for
tax withholding
— — (6.3)— — (6.3)— 
Preferred dividend ($12.50 per
share of redeemable preferred
stock)
— — — (8.1)— (8.1)— 
Net earnings— — — 45.5 — 45.5 — 
Other comprehensive loss, net of
tax
— — — — 25.4 25.4 — 
Balance at December 31, 2019146,359.5 $1.5 $2,759.2 $(694.0)$(350.6)$1,716.1 $606.6 
2020
Shares of Common StockCommon StockAdditional Paid in CapitalAccumulated DeficitAccumulated Other Comprehensive LossTotal Shareholders' EquityRedeemable Preferred Stock
Balance at September 30, 2020164,567 $2 $3,901 $(461)$(370)$3,072 $607 
Share issuances related to stock-
     based compensation
174 — — — — — — 
Conversion of redeemable
     preferred stock
5,392 — 253 — — 253 (248)
Stock-based compensation— — 12 — — 12 — 
Cash paid, in lieu of equity, for
     tax withholding
— — (7)— — (7)— 
Employee stock purchase plan— — — — — 
Preferred dividend ($12.50 per
     share of redeemable preferred
     stock)
— — — (4)— (4)— 
Net earnings— — — 88 — 88 — 
Other comprehensive income, net
       of tax
— — — — 40 40 — 
Balance at December 31, 2020170,133 $2 $4,161 $(377)$(330)$3,456 $359 



The accompanying notes are an integral part of these unaudited consolidated financial statements.
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Catalent, Inc.
Consolidated Statement of Changes in Shareholders' Equity
(Unaudited; dollars in millions, except share data in thousands)


Six months ended December 31, 2021
Shares of Common StockCommon StockAdditional Paid in CapitalRetained EarningsAccumulated Other Comprehensive LossTotal Shareholders' EquityRedeemable Preferred Stock
Balance at June 30, 2021170,549 $2 $4,205 $25 $(317)$3,915 $359 
Share issuances related to stock-
     based compensation
683 — — — — — — 
Conversion of redeemable
     preferred stock
7,818 — 362 — — 362 (359)
Stock-based compensation— — 32 — — 32 — 
Cash paid, in lieu of equity, for
     tax withholding
— — (9)— — (9)— 
Exercise of stock options— — 19 — — 19 — 
Employee stock purchase plan— — — — — 
Preferred dividend ($12.50 per
     share of redeemable preferred
     stock)
— — — (6)— (6)— 
Net earnings— — — 190 — 190 — 
Other comprehensive loss, net of
tax
— — — — (28)(28)— 
Balance at December 31, 2021179,050 $2 $4,615 $209 $(345)$4,481 $ 

Six Months Ended December 31, 2020

Shares of Common StockCommon StockAdditional Paid in CapitalAccumulated DeficitAccumulated Other Comprehensive LossTotal Shareholders' EquityRedeemable Preferred Stock
Balance at June 30, 2020162,788 $2 $3,819 $(535)$(387)$2,899 $607 
Equity offering, sale of common
     stock
1,163 — 82 — — 82 — 
Share issuances related to stock-
     based compensation
790 — — — — — — 
Conversion of redeemable
     preferred stock
5,392 — 253 — — 253 (248)
Stock-based compensation— — 30 — — 30 — 
Cash paid, in lieu of equity, for
     tax withholding
— — (27)— — (27)— 
Employee stock purchase plan— — — — — 
Preferred dividend ($12.50 per
     share of redeemable preferred
     stock)
— — — (13)— (13)— 
Net earnings— — — 171 — 171 — 
Other comprehensive income,
net of tax
— — — — 57 57 — 
Balance at December 31, 2020170,133 $2 $4,161 $(377)$(330)$3,456 $359 




The accompanying notes are an integral part of these unaudited consolidated financial statements.
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Catalent, Inc. and Subsidiaries
Consolidated StatementStatements of Changes in Shareholders' EquityCash Flows
(Unaudited; dollars in millions, except share data in thousands)

millions)
Six months ended December 31, 2020
Shares of Common StockCommon StockAdditional Paid in CapitalAccumulated DeficitAccumulated Other Comprehensive LossTotal Shareholders' EquityRedeemable Preferred Stock
Balance at June 30, 2020162,788.0 $1.6 $3,818.7 $(535.2)$(386.3)$2,898.8 $606.6 
Equity offering, sale of common
stock
1,162.5 — 81.8 — — 81.8 — 
Share issuances related to stock-
     based compensation
790.5 — — — — — 
Conversion of redeemable
preferred stock
5,392.3 0.1 252.9 — — 253.0 (247.6)
Stock-based compensation— — 30.1 — — 30.1 — 
Cash paid, in lieu of equity, for
tax withholding
— — (26.4)— — (26.4)— 
Employee stock purchase plan— — 3.7 — — 3.7 — 
Preferred dividend ($12.50 per
share of redeemable preferred
stock)
— — — (13.0)— (13.0)— 
Net earnings— — — 170.8 — 170.8 — 
Other comprehensive income, net
of tax
— — — — 56.7 56.7 — 
Balance at December 31, 2020170,133.3 $1.7 $4,160.8 $(377.4)$(329.6)$3,455.5 $359.0 

Six Months Ended December 31, 2019
Shares of Common StockCommon StockAdditional Paid in CapitalAccumulated DeficitAccumulated Other Comprehensive LossTotal Shareholders' EquityRedeemable Preferred Stock
Balance at June 30, 2019145,738.3 $1.5 $2,757.4 $(723.4)$(353.9)$1,681.6 $606.6 
Share issuances related to stock-
     based compensation
621.2 — — — — — 
Stock-based compensation— — 26.9 — — 26.9 
Cash paid, in lieu of equity, for
tax withholding
— — (24.4)— — (24.4)— 
Non-qualified stock— — (0.7)— — (0.7)— 
Preferred dividend ($12.50 per
share of redeemable preferred
stock)
— — — (16.2)— (16.2)— 
Net earnings— — — 45.6 — 45.6 — 
Other comprehensive income, net
of tax
— — — — 3.3 3.3 — 
Balance at December 31, 2019146,359.5 $1.5 $2,759.2 $(694.0)$(350.6)$1,716.1 $606.6 




Six Months Ended December 31,
20212020
CASH FLOWS FROM OPERATING ACTIVITIES:
Net earnings$190 $171 
Adjustments to reconcile net earnings to net cash from operations:
Depreciation and amortization179 140 
Non-cash foreign currency transaction loss (gain), net25 (12)
Amortization of debt issuance costs
Impairments charges and loss (gain) on sale of assets19 
Gain on sale of subsidiary(1)— 
Financing-related charges— 
Gain on derivative instrument(2)(16)
Stock-based compensation32 30 
Provision for (benefit from) deferred income taxes(5)
Provision for bad debts and inventory18 
Change in operating assets and liabilities:
Decrease in trade receivables131 88 
Increase in inventories(148)(140)
Increase in accounts payable14 
Other assets/accrued liabilities, net—current and non-current(214)(69)
Net cash provided by operating activities232 224 
CASH FLOWS USED IN INVESTING ACTIVITIES:
Acquisition of property, equipment, and other productive assets(277)(339)
Proceeds from maturity of marketable securities— 
Settlement on sale of subsidiaries, net(3)— 
Payment for acquisitions, net of cash acquired(1,020)(14)
Payment made for investments(3)(1)
Net cash used in investing activities(1,299)(354)
CASH FLOWS FROM FINANCING ACTIVITIES:
Proceeds from borrowings1,100 
Payments related to long-term obligations(64)(55)
Financing fees paid(15)— 
Dividends paid(4)(13)
Proceeds from sale of common stock, net— 82 
Cash paid, in lieu of equity, for tax-withholding obligations(9)(27)
Exercise of stock options19 — 
Other financing activities
Net cash provided by (used in) financing activities1,033 (7)
Effect of foreign currency exchange on cash and cash equivalents(13)17 
NET DECREASE IN CASH AND CASH EQUIVALENTS(47)(120)
CASH AND CASH EQUIVALENTS AT BEGINNING OF PERIOD896 953 
CASH AND CASH EQUIVALENTS AT END OF PERIOD$849 $833 
SUPPLEMENTARY CASH FLOW INFORMATION:
Interest paid$50 $52 
Income taxes paid, net$27 $19 
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,
20202019
CASH FLOWS FROM OPERATING ACTIVITIES:
Net earnings$170.8 $45.6 
Adjustments to reconcile net earnings to net cash from operations:
Depreciation and amortization140.1 122.5 
Non-cash foreign currency transaction (gain) loss, net(12.0)5.5 
Amortization and write-off of debt financing costs3.3 3.1 
Asset impairments charges and (gain) loss on sale of assets2.4 1.5 
Gain on derivative instrument(16.0)(1.4)
Stock-based compensation30.1 26.9 
(Benefit from) provision for deferred income taxes(5.3)2.7 
Provision for bad debts and inventory18.4 9.4 
Change in operating assets and liabilities:
Decrease in trade receivables87.6 4.3 
Increase in inventories(140.3)(11.6)
Increase (decrease) in accounts payable13.4 (13.3)
Other assets/accrued liabilities, net—current and non-current(68.8)(49.3)
Net cash provided by operating activities223.7 145.9 
CASH FLOWS FROM INVESTING ACTIVITIES:
Acquisition of property, equipment, and other productive assets(338.9)(152.2)
Proceeds from sale of property and equipment0.3 
Proceeds from sale of subsidiaries20.8 
Payment for acquisitions, net of cash acquired(14.8)(10.7)
Payment made for investments(1.0)(2.0)
Prepayment for pending business acquisition(55.1)
Net cash used in investing activities(354.4)(199.2)
CASH FLOWS FROM FINANCING ACTIVITIES:
Net change in other borrowings1.5 (5.9)
Payments related to long-term obligations(54.8)(51.5)
Dividends paid(13.0)(20.0)
Proceeds from sale of common stock, net81.8 
Cash paid, in lieu of equity, for tax-withholding obligations(26.4)(24.4)
Other financing activities3.7 
Net cash used in financing activities(7.2)(101.8)
Effect of foreign currency exchange on cash17.8 (1.4)
NET DECREASE IN CASH AND EQUIVALENTS(120.1)(156.5)
CASH AND EQUIVALENTS AT BEGINNING OF PERIOD953.2 345.4 
CASH AND EQUIVALENTS AT END OF PERIOD$833.1 $188.9 
SUPPLEMENTARY CASH FLOW INFORMATION:
Interest paid$52.0 $47.7 
Income taxes paid, net$18.9 $19.6 



The accompanying notes are an integral part of these unaudited consolidated financial statements.
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Catalent, Inc. and Subsidiaries
Notes to Unaudited Consolidated Financial Statements
1.    BASIS OF PRESENTATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Business
Catalent, Inc. (Catalent or the Company) directly and wholly owns PTS Intermediate Holdings LLC (Intermediate Holdings). Intermediate Holdings directly and wholly owns Catalent Pharma Solutions, Inc. (Operating 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 (“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 six months ended December 31, 20202021 are not necessarily indicative of the results that may be expected for the year ending June 30, 2021.2022. The consolidated balance sheet at June 30, 20202021 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 footnotes thereto included in the Company’s Annual Report on Form 10-K for the year ended June 30, 20202021 filed with the Securities and Exchange Commission.Commission (the “SEC”).

Reclassifications

Certain prior period balances have been reclassified to conform to the current period presentation. These reclassifications did not have a material impact on the consolidated statements of operations, consolidated balance sheets, consolidated statements of cash flows, or notes to the consolidated financial statements.

Foreign Currency Translation
The financial statements of the Company’s operations are generally measured using the local currency as the functional currency. Adjustments to translate the assets and liabilities of operations outside the U.S. into U.S. dollars are accumulated as a component of other comprehensive income utilizing period-end exchange rates. Since July 1, 2018, the Company has accounted for its Argentine operations as highly inflationary.
AllowanceDepreciation
Depreciation expense was $64 million and $48 million for Credit Losses

Trade receivablesthe three months ended December 31, 2021 and contract2020, respectively. Depreciation expense was $122 million and $94 million for the six months ended December 31, 2021 and 2020, respectively. Depreciation expense includes amortization of assets are primarily comprised of amounts owedrelated to the Company through its operating activities and are presented net of an allowance that includes an assessment of expected credit losses.finance leases. The Company determines its allowance methodology by considering various factors, including the Company’s previous loss history, significant changes in a geographic location's economic conditions,charges repairs and the current and future condition of the general economy and the industry in which the Company's customers operate. To the extent that any individual payer is identified whose credit quality has deteriorated, the Company establishes allowances based on the individual risk characteristics of such customer. The Company makes concerted effortsmaintenance costs to collect all outstanding balances due from customers; however, trade receivables and contract assets are written off against the allowance when the related balances are no longer deemed collectible.expense as incurred.
Research and Development Costs
The Company expenses research and development costs as incurred. Research and development costs amounted to $5.2$6 million and $4.9$5 million for the three months ended December 31, 20202021 and 2019,2020, respectively. Research and development costs amounted to $11.6 million and $9.5$12 million for the six months ended December 31, 20202021 and 2019, respectively.2020.
Marketable Securities

The Company classifies its marketable securities as available-for-sale, because it may sell certain of its marketable securities prior to the stated maturity for various reasons, including management of liquidity, credit risk, duration, relative return, and asset allocation. The Company determines the fair value of each marketable security in its portfolio at each period end and recognizes gains and losses in the portfolio in other comprehensive income. As of December 31, 2021, the amortized cost basis of marketable securities approximates fair value and all outstanding marketable securities mature within one year.
Recent Financial Accounting Standards
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Recently Adopted Accounting Standards
In August 2018,December 2019, the Financial Accounting Standards Board (the “FASB”) issued Accounting Standards Update (“ASU”) 2018-15, 2019-12Intangibles—Goodwill and Other—Internal-Use Software (Subtopic 350-40), Income Taxes (Topic 740): Customer'sSimplifying the Accounting for Implementation Costs Incurred in a Cloud Computing Arrangement That Is a Service ContractIncome Taxes, which alignseliminates certain exceptions related to the requirementsincremental approach for capitalizing implementation costs incurredintra-period allocation, deferred tax recognition requirement for changes in a hosting arrangement that is a service contract with
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equity method investments and non-U.S. subsidiaries, and methodology for calculating income taxes in an interim period. The guidance also simplifies certain aspects of the requirementsaccounting for capitalizing implementation costs incurred to developfranchise taxes, the accounting for step-up in the tax basis of goodwill, and accounting for the change in the enacted change in tax laws or obtain internal-use software.rates. The Company adopted the guidance on July 1, 2020.2021. The adoption of this guidance did not have a material impact on the Company’s financial condition or results of operations.
In August 2018, the FASB issued ASU 2018-13, Fair Value Measurement (Topic 820)2018-14, Compensation—Retirement Benefits—Defined Benefit Plans—General (Subtopic 715-20): Disclosure Framework—Changes to the Disclosure RequirementRequirements for Fair Value Measurement,Defined Benefit Plan, which changesremoves certain disclosures and added additional disclosures around weighted-average interest crediting rates for cash balance plans and explanation for significant gains and losses related to change in the disclosure requirements on fair value measurements in Accounting Standards Codification (ASC”) 820 Fair Value Measurement. The guidance eliminates certain disclosure requirements that are no longer considered cost beneficial and adds new disclosure requirementsbenefit obligation for Level 3 fair value measurements.the period. The Company adopted the guidance on July 1, 2020.2021. The adoption of this guidance did not have a material impact on the Company’s consolidated financial condition or results of operations.
In June 2016, the FASB issued ASU 2016-13, Financial Instruments—Credit Losses (Topic 326): Measurement of Credit Losses on Financial Instruments, which introduces a new accounting model known as Credit Expected Credit Losses (“CECL”). CECL requires earlier recognition of credit losses on financial assets, while also providing additional transparency about credit risk. The CECL model utilizes a lifetime expected credit loss measurement objective for the recognition of credit losses for financial assets at the time they are originated or acquired. The expected credit losses are adjusted each period for changes in expected lifetime credit losses. This model replaces the multiple existing impairment models in current U.S. GAAP, which generally require that a loss be incurred before it is recognized. The new standard applies to receivables arising from revenue transactions such as contract assets and accounts receivables. The Company adopted the amended guidance using a modified retrospective approach on July 1, 2020. The amended guidance did not have a material impact on the Company’s financial condition or results of operations.statements.
New Accounting Standards Not Adopted as of December 31, 20202021
In March 2020, the FASB issued ASU 2020-04, Reference Rate Reform (Topic 848): Facilitation of the Effects of Reference Rate Reform on Financial Reporting, which provides optional guidance to ease the potential burden in accounting for the discontinuation of a reference rate such as LIBOR, formerly known as the London Interbank Offered Rate, because of reference rate reform. The expedients and exceptions provided by the guidance do not apply to contract modifications made and hedging relationships entered into or evaluated after December 31, 2022. The ASU is effective for all entities as of March 12, 2020 through December 31, 2022. The Company is currently evaluating the impact of adopting this guidance on its consolidated financial statements.
In December 2019, the FASB issued ASU 2019-12, Income Taxes (Topic 740): Simplifying the Accounting for Income Taxes, which eliminates certain exceptions related to the incremental approach for intra-period allocation, deferred tax recognition requirement for changes in equity method investments and foreign subsidiaries, and methodology for calculating income taxes in an interim period. The guidance also simplifies certain aspects of the accounting for franchise taxes, the accounting for step-up in the tax basis of goodwill, and accounting for the change in the enacted change in tax laws or rates. The ASU will be effective for fiscal years beginning after December 15, 2020 and interim periods within those fiscal years. The Company is currently evaluating the impact of adopting this guidance on its consolidated financial statements.

2.    REVENUE RECOGNITION
The Company recognizes revenue in accordance with ASCAccounting Standards Codification (“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.
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 allocate revenue for the three and six months ended December 31, 20202021 and December 31, 2019,2020, by type of activity and reporting segment (in millions):
Three Months Ended December 31, 2021BiologicsSoftgel and Oral TechnologiesOral and Specialty DeliveryClinical Supply ServicesTotal
Manufacturing & commercial product supply$169 $289 $96 $— $554 
Development services469 40 60 — 569 
Clinical supply services— — — 99 99 
Total$638 $329 $156 $99 $1,222 
Inter-segment revenue elimination(5)
Combined net revenue$1,217 
Three Months Ended December 31, 2020BiologicsSoftgel and Oral TechnologiesOral and Specialty DeliveryClinical Supply ServicesTotal
Manufacturing & commercial product supply$124 $214 $114 $— $452 
Development services280 33 56 — 369 
Clinical supply services— — — 93 93 
Total$404 $247 $170 $93 $914 
Inter-segment revenue elimination(3)
Combined net revenue$911 

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Three Months Ended December 31, 2020BiologicsSoftgel & Oral TechnologiesOral & Specialty DeliveryClinical Supply ServicesTotal
Six Months Ended December 31, 2021Six Months Ended December 31, 2021BiologicsSoftgel and Oral TechnologiesOral and Specialty DeliveryClinical Supply ServicesTotal
Manufacturing & commercial product supplyManufacturing & commercial product supply$124.4 $213.8 $113.5 $$451.7 Manufacturing & commercial product supply$303 $496 $184 $— $983 
Development servicesDevelopment services279.5 32.8 56.4 368.7 Development services881 76 118 — 1,075 
Clinical supply servicesClinical supply services93.5 93.5 Clinical supply services— — — 195 195 
TotalTotal$403.9 $246.6 $169.9 $93.5 $913.9 Total$1,184 $572 $302 $195 $2,253 
Inter-segment revenue elimination(3.1)Inter-segment revenue elimination(11)
Combined net revenue$910.8 Combined net revenue$2,242 

Three Months Ended December 31, 2019BiologicsSoftgel & Oral TechnologiesOral & Specialty DeliveryClinical Supply ServicesTotal
Six Months Ended December 31, 2020Six Months Ended December 31, 2020BiologicsSoftgel and Oral TechnologiesOral and Specialty DeliveryClinical Supply ServicesTotal
Manufacturing & commercial product supplyManufacturing & commercial product supply$80.0 $245.0 $91.4 $$416.4 Manufacturing & commercial product supply$214 $405 $217 $— $836 
Development servicesDevelopment services145.2 22.9 51.8 219.9 Development services567 63 111 — 741 
Clinical supply servicesClinical supply services87.9 87.9 Clinical supply services— — — 186 186 
TotalTotal$225.2 $267.9 $143.2 $87.9 $724.2 Total$781 $468 $328 $186 $1,763 
Inter-segment revenue elimination(2.8)Inter-segment revenue elimination(6)
Combined net revenue$721.4 Combined net revenue$1,757 

Six Months Ended December 31, 2020BiologicsSoftgel & Oral TechnologiesOral and Specialty DeliveryClinical Supply ServicesTotal
Manufacturing & commercial product supply$214.3 $404.4 $217.0 $$835.7 
Development services566.7 63.3 111.2 741.2 
Clinical supply services186.2 186.2 
Total$781.0 $467.7 $328.2 $186.2 $1,763.1 
Inter-segment revenue elimination(6.6)
Combined net revenue$1,756.5 

Six Months Ended December 31, 2019BiologicsSoftgel & Oral TechnologiesOral and Specialty DeliveryClinical Supply ServicesTotal
Manufacturing & commercial product supply$144.4 $483.9 $167.3 $$795.6 
Development services269.4 44.6 108.5 422.5 
Clinical supply services172.5 172.5 
Total$413.8 $528.5 $275.8 $172.5 $1,390.6 
Inter-segment revenue elimination(4.5)
Combined net revenue$1,386.1 

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The following table allocates revenue by the location where the goods were made or the service performed:

Three Months Ended
December 31,
Six Months Ended 
December 31,
Three Months Ended
December 31,
Six Months Ended 
December 31,
(Dollars in millions)(Dollars in millions)2020201920202019(Dollars in millions)2021202020212020
United StatesUnited States$535.3 $414.7 $1,052.2 $777.0 United States$793 $535 $1,423 $1,052 
EuropeEurope326.4 239.5 609.9 458.6 Europe370326722 610 
International Other72.0 87.3 138.7 189.1 
OtherOther8372155 139 
Elimination of revenue attributable to multiple locationsElimination of revenue attributable to multiple locations(22.9)(20.1)(44.3)(38.6)Elimination of revenue attributable to multiple locations(29)(22)(58)(44)
TotalTotal$910.8 $721.4 $1,756.5 $1,386.1 Total$1,217 $911 $2,242 $1,757 
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Contract Liabilities
Contract liabilities relate to cash consideration that the Company receives in advance of satisfying the related performance obligations. The contract liabilities balance (current and non-current) as of December 31, 20202021 and June 30, 20202021 are as follows:
(Dollars in millions)
Balance at June 30, 20202021$218.4321 
Balance at December 31, 20202021$273.1289 
Revenue recognized in the period from July 1 through December 31, 2020:
Amountsamounts included in contractcontracts liability at the beginning of the periodperiod:$49.4182 

Contract liabilities that will be recognized within 12 months of December 31, 2021 are accounted for in Other accrued liabilities and those that will be recognized longer than 12 months after December 31, 2021 are accounted for within Other liabilities.

Contract Assets
Contract assets primarily relate to the Company's conditional right to receive consideration for services that have been performed for a customercustomers as of December 31, 20202021 relating to the Company's development services but had not yet been invoiced as of December 31, 2020.2021. Contract assets are transferred to trade receivables, net when the Company’s right to receive the consideration becomes unconditional. Contract assets totaled $122.9$308 million and $61.4181 million as of December 31, 20202021 and June 30, 2020,2021, respectively. Contract assets are included in Prepaidprepaid expenses and other as they are expected to be transferred to trade receivables within 12 months of December 31, 2020.in the consolidated balance sheets.
3.    BUSINESS COMBINATIONS AND DIVESTITURES
Anagni Acquisition
In January 2020, the Company acquired an oral solid, biologics, and sterile product manufacturing and packaging facility in Anagni, Italy (“Anagni”) from a unit of Bristol-Myers Squibb Company (“BMS”). The Company paid to BMS $55.3 million in cash as part of the purchase consideration and as consideration for the provision of certain services to facilitate the transition from BMS to Company ownership. At the closing of this acquisition, BMS also entered into a five-year agreement for continuing supply by the Company of certain products formerly produced by BMS at the Anagni facility. Due to the variety of activities performed at Anagni, the results of the Anagni facility are allocated between the Oral and Specialty Delivery and Biologics segments.
The total cash consideration was allocated between the facility purchase and the transitional services arrangement, with $52.2 million assigned to the purchase consideration and the balance to transitional services. The Company funded the entire purchase price with cash on hand and has allocated the purchase price among the acquired assets, recognizing property, plant, and equipment of $34.2 million, inventory of $6.5 million, and prepaid expenses and other of $12.2 million. The remainder of the value was allocated to deferred tax assets and certain employee-related liabilities assumed in the acquisition.
Masthercell Global Inc. Acquisition

In February 2020, the Company acquired 100% of the equity interest in Masthercell Global Inc. (“MaSTherCell”) for an aggregate purchase price of $323.3 million, subject to adjustment, which was funded with the net proceeds of the Company’s February 2020 public offering (the “February 2020 Equity Offering”) of its common stock, par value $0.01 (“Common Stock”). See Note 13, Equity, Redeemable Preferred Stock and Accumulated Other Comprehensive Loss. MaSTherCell is a contract
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development and manufacturing organization focused on the development and manufacture of autologous and allogeneic cell therapies for third parties, as well as a variety of related analytical services.

The Company accounted for the MaSTherCell acquisition using the acquisition method in accordance with ASC 805. The operating results of MaSTherCell have been included in the Company’s consolidated financial statements for the period following the acquisition date.

The Company preliminarily 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 as part of the MaSTherCell acquisition. The Company recognized, property, plant and equipment of $25.5 million, $51.0 million for identifiable intangible assets, $2.0 million for other net assets, and $7.7 million for deferred income tax liabilities. The remainder of the fair value, $252.5 million, was preliminarily allocated to goodwill. Goodwill is mainly comprised of the growth from an expected increase in capacity utilization, potential new customers, and advanced cell therapy development and manufacturing capabilities.
During the measurement period ending no later than one year after the acquisition date, the Company has continued to obtain information to assist in finalizing the fair values of the net assets acquired, which have not differed materially from these preliminary estimates. The amounts subject to finalization include working capital and income taxes. If any remaining measurement period adjustment is material, the Company will record such adjustment, including any related impact on net income, prior to the expiration of the measurement period.
Skeletal Cell Therapy Support SA Acquisition

In November 2020, the Company acquired 100% of the equity interest in Skeletal Cell Therapy Support SA (“Skeletal”) from Bone Therapeutics SA (“Bone”) for $14.8$15 million, subject to customary adjustments, as well as related supply agreements with Bone.the seller. Skeletal operates a cell therapy manufacturing facility in Gosselies, Belgium. The facility and operations are part ofwere assigned to the Company’s Biologics segment, expanding the Company’s cell therapy capacity for clinical and commercial supply. The acquisition, when combined with the Company's other European-based facilities and capabilities in cell therapy, will createhas created an integrated European center of excellence in cell therapy.
The Company accounted for the Skeletal acquisition using the acquisition method in accordance with ASC 805, Business Combinations. The Company funded the entire purchase price with cash on hand and allocated the purchase price among the acquired assets, recognizing goodwill of $9 million. The Company allocated the remainder of the purchase price to trade receivables, property, plant, and equipment, and other current and non-current assets and liabilities assumed in the acquisition. Results for the three and six months ended December 31, 2021 were not material to the Company’s statement of operations, financial position, or cash flows.
Acorda Therapeutics, Inc. Acquisition
In February 2021, the Company acquired the manufacturing and packaging operations of the Acorda Therapeutics, Inc. (“Acorda”) dry powder inhaler and spray dry manufacturing business, including its manufacturing facility located near Boston, Massachusetts, for $83 million, subject to customary adjustments. In connection with the purchase, Acorda and the Company entered into a long-term supply agreement, under which the Company will continue the manufacture and packaging of an Acorda product at the facility. The facility and operations became part of the Company’s Oral and Specialty Delivery segment. Results of the business acquired were not material to the Company's statement of operations, financial position, or cash flows for the three and six months ended December 31, 2021.

The Company accounted for the Skeletal acquisitionAcorda transaction using the acquisition method in accordance with ASC 805. The Company funded the entire purchase price with cash on hand and has preliminarily allocated the purchase price among the acquired assets, recognizing property, plant, and equipment of $8.7$79 million, inventory of $2 million, and goodwill of $5.4$2 million. The remainder of the valuepurchase price was preliminarily allocated to trade receivables, and to other current and non-current assets and liabilities assumed in the acquisition.

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The Company has not completed its analysis regarding the assets acquired and liabilities assumed. Therefore, the allocation to goodwill and inventory are preliminary and subject to finalization. The Company expects to finalize its allocation within one year from the acquisition date.
Delphi Genetics SA Acquisition
In February 2021, the Company acquired 100% of the equity interest in Delphi Genetics SA (“Delphi”) for $50 million, subject to customary adjustments. Delphi is a plasmid DNA (pDNA) cell and gene therapy contract development and manufacturing organization based in Gosselies, Belgium. The facility and operations acquired became part of the Company’s Biologics segment. Results of the business acquired were not material to the Company's statement of operations, financial position, or cash flows for the three and six months ended December 31, 2021.
The Company accounted for the Delphi transaction using the acquisition method in accordance with ASC 805. The Company funded the entire purchase price with cash on hand and allocated the purchase price among the acquired assets, recognizing property, plant, and equipment of $4 million, intangible assets of $7 million, other current assets of $3 million, assumed debt of $6 million, other current liabilities of $1 million, and goodwill of $43 million.
Hepatic Cell Therapy Support SA Asset Acquisition
In April 2021, the Company acquired 100% of the equity interest in Hepatic Cell Therapy Support SA (“Hepatic”) for approximately $15 million, net of cash acquired and debt assumed. Hepatic operates a manufacturing facility at the same location where Skeletal operates a cell therapy manufacturing facility in Gosselies, Belgium. The acquired facility expands the Company’s cell therapy capacity for clinical and commercial supply in its Biologics segment.
The Company accounted for the Hepatic transaction as an asset acquisition in accordance with ASC 805. The Company funded the entire purchase price with cash on hand and allocated the purchase price to the assets acquired and liabilities assumed, recognizing property, plant, and equipment of $13 million, other current and non-current assets of $3 million, and assumed debt of $1 million.
RheinCell Therapeutics GmbH Acquisition

In August 2021, the Company acquired 100% of the equity interest in RheinCell Therapeutics GmbH (“RheinCell”) for approximately $26 million, net of cash acquired. RheinCell is a developer and manufacturer of induced pluripotent stem cells (“iPSCs”), including iPSCs meeting current good manufacturing practices (“CGMP”) standards, based in Lagenfeld, Germany. The operations became part of the Company’s Biologics segment and builds upon Catalent’s existing custom cell therapy process development and manufacturing capabilities with proprietary CGMP cell lines for iPSC-based therapies.
The Company accounted for the RheinCell transaction using the acquisition method in accordance with ASC 805. The Company funded the entire purchase price with cash on hand and preliminarily allocated the purchase price among the assets acquired, recognizing of $2 million of current assets, $3 million of other assets, $4 million of current liabilities, $5 million of other liabilities, $14 million of intangible assets, and goodwill of $16 million. Results of this business were not material to the Company's statement of operations, financial position, or cash flows for the three and six months ended December 31, 2021.
The Company has not completed its analysis regarding the assets acquired and liabilities assumed. Therefore, the allocation to goodwill and income taxes are preliminary and subject to finalization. The Company expects to finalize its allocation over the next several months, but, in any event, within one year from the closing.acquisition date.
Blow-Fill-Seal Divestiture AgreementBettera Holdings, LLC Acquisition

In December 2020,October 2021, the Company entered intoacquired 100% of the equity interest in Bettera Holdings, LLC (“Bettera”) for approximately $1 billion, subject to customary adjustments. Bettera is a Stockmanufacturer of nutraceuticals and Asset Purchase Agreementnutritional supplements in gummy, soft chew, and lozenge delivery formats.
The Company accounted for the Bettera transaction using the acquisition method in accordance with ASC 805. 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. The Company has not completed its analysis regarding the assets acquired and liabilities assumed. Therefore, the allocation to current liabilities, property, plant, and equipment, intangible assets, goodwill, and income taxes are preliminary and subject to finalization. During the measurement period ending no later than one year after the acquisition date, the Company will continue to obtain information to assist in finalizing the fair values of the net assets acquired, which may differ materially from these preliminary estimates. If any measurement period adjustment is material, the Company will record such adjustment, including any related impact on net income, in the reporting period in which the adjustment is determined.
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The preliminary purchase price allocation to assets acquired and liabilities assumed in the transaction, subject to finalization, is as follows:

(Dollars in millions)Preliminary Purchase Price Allocation
Cash and cash equivalents$23 
Trade receivables, net16 
Inventories32 
Other current assets
Property, plant, and equipment73 
Other intangibles, net (1)
361 
Other assets
Current liabilities(21)
Goodwill528 
Total assets acquired and liabilities assumed$1,017 
(1) Other intangibles, net includes core technology of $338 million and customer relationships of $23 million.
The carrying value of trade receivables, 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 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.
Core technology intangible assets of $338 million were valued using the multi-period, excess-earnings method, a subsidiarymethod that values the intangible asset using the present value of SK Capital Partners, LPthe after-tax cash flows attributable to sell the Company’s blow-fill-seal manufacturingintangible 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 that appropriately reflects the risk inherent in each future cash flow stream, and 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-comparable information. Fair-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 core technology intangible asset has a weighted average useful life of 10 years.
Goodwill has been allocated to the Softgel and Oral Technologies segment as shown in Note 4, Goodwill. Goodwill is mainly comprised of the growth from an expected increase in capacity utilization and potential new customers. The goodwill resulting from the Bettera acquisition is deductible for tax purposes.
Results of the business includingacquired were not material to the Company's consolidated statement of operations, financial position, or cash flows for the three months ended December 31, 2021.
Blow-Fill-Seal Divestiture
In March 2021, the Company sold 100% of the shares of Catalent USA Woodstock, Inc. (theand certain related assets (collectively, the “Blow-Fill-Seal Business”), to a subsidiary of SK Capital Partners, LP for $300.0$300 million in cash, and a $50.0$50 million note receivable (estimated fair value of $47 million) as well as potential additional contingent consideration (up to $50.0$50 million) based on future events concerningdependent upon the performance of aspects of the Blow-Fill-Seal Business. The Stock and Asset Purchase Agreement is subject to customary closing conditions and is expected to close before the end of fiscal 2021. The Blow-Fill-Seal Business iswas part of the Oral and Specialty Delivery segment. The carrying value of the net assets sold was $149 million, which included goodwill of $54 million. As a result of the sale, the Company realized a gain from sale of subsidiary of $182 million, net of transaction costs, for the fiscal year ended June 30, 2021.
During the six months ended December 31, 2020,2021, the Company settled a post-closing purchase price adjustment, which resulted in a gain on sale of subsidiary of $1 million.
All consideration received was measured at its divestiture date fair value. The Company valued the total consideration received from divestiture of the Blow-Fill-Seal Business met the criteria to be classified as held for sale; as a result, these assets and liabilities have been reclassified within the consolidated balance sheet as of December 31, 2020. Refer to Note 4, Goodwill and Note 16, Supplemental Balance Sheet Information for more details.

follows:
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(Dollars in millions)Fair value of consideration received
Cash, gross$300 
Note receivable (1)
47 
Contingent consideration (2)
— 
Other (3)
(16)
Total$331 

(1)    The note receivable, which provides for interest at a rate of 5.0% paid in kind, had an estimated fair value of $47 million, which is the $50 million aggregate principal amount less a $3 million discount determined using a discounted cash flow model with the market interest rate as a significant input.
(2)    The Company determined that the estimated fair value of the contingent consideration from the sale of the Blow-Fill-Seal Business at December 31, 2021 is zero, and therefore, no contingent consideration was recorded as a result of the divestiture of the Blow-Fill-Seal Business. If any contingent consideration is subsequently received, it will be recorded in the period in which it is received. The Company has elected an accounting policy to recognize increases in the carrying amount of the contingent consideration asset using the gain contingency guidance in ASC 450, Contingencies.
(3)    Other includes $8 million of transaction expenses, a working capital adjustment of $6 million, and a $2 million assumption of liabilities to create cumulative net cash proceeds of $284 million.
4.    GOODWILL
The following table summarizes the changes between June 30, 20202021 and December 31, 20202021 in the carrying amount of goodwill in total and by reporting segment:
(Dollars in millions)BiologicsSoftgel and Oral TechnologiesOral and Specialty DeliveryClinical Supply ServicesTotal
Balance at June 30, 2021$1,531 $516 $316 $156 $2,519 
Additions(1)
14 528 — — 542 
Foreign currency translation adjustments(17)(11)(4)(3)(35)
Balance at December 31, 2021$1,528 $1,033 $312 $153 $3,026 

(Dollars in millions)BiologicsSoftgel & Oral TechnologiesOral & Specialty DeliveryClinical Supply ServicesTotal
Balance at June 30, 2020$1,462.2 $505.5 $354.7 $148.2 $2,470.6 
Additions(1)
5.4 5.4 
Classified as held for sale(2)
(65.6)(65.6)
Other(3)
(1.4)0.1 (1.3)
Foreign currency translation adjustments20.7 15.3 9.7 6.7 52.4 
Balance at December 31, 2020$1,486.9 $520.8 $298.9 $154.9 $2,461.5 
(1) The additionadditions to goodwill inarise from the Biologics reporting segment relates to the Skeletal transaction. SeeBettera (Softgel and Oral Technologies) and RheinCell and Delphi (Biologics) acquisitions. For further details, see Note 3, Business Combinations and Divestitures.
(2) Represents goodwill associated with the Company's Blow-Fill-Seal Business.
(3) The change in Other in the Biologics reporting segment primarily relates to the MaSTherCell transaction.
The Company recorded no impairment charge to goodwill in the current period.

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5.    DEFINITE-LIVED LONG-LIVED ASSETS

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The Company’s definite-lived long-lived assets include property, plant, and equipment as well as intangible assets with definite lives. Refer to Note 16, 5.    OTHER INTANGIBLES, NETSupplemental Balance Sheet Information for details related to property, plant, and equipment.
The details of other intangibles net as of December 31, 20202021 and June 30, 20202021 are as follows:
(Dollars in millions)(Dollars in millions)Weighted Average Life
Gross
Carrying
Value
Accumulated
Amortization
Net
Carrying
Value
(Dollars in millions)Weighted Average Life
Gross
Carrying
Value
Accumulated
Amortization
Net
Carrying
Value
December 31, 2020
December 31, 2021December 31, 2021
Amortized intangibles:Amortized intangibles:Amortized intangibles:
Core technologyCore technology19 years$140.9 $(90.9)$50.0 Core technology11 years$487 $(104)$383 
Customer relationshipsCustomer relationships14 years1,039.3 (292.4)746.9 Customer relationships13 years1,037 (337)700 
Product relationshipsProduct relationships11 years280.0 (231.4)48.6 Product relationships8 years249 (209)40 
OtherOther5 years16.3 (6.5)9.8 Other5 years19 (10)
Total intangible assets$1,476.5 $(621.2)$855.3 
Total other intangiblesTotal other intangibles$1,792 $(660)$1,132 

(Dollars in millions)(Dollars in millions)Weighted Average Life
Gross
Carrying
Value
Accumulated
Amortization
Net
Carrying
Value
(Dollars in millions)Weighted Average Life
Gross
Carrying
Value
Accumulated
Amortization
Net
Carrying
Value
June 30, 2020
June 30, 2021June 30, 2021
Amortized intangibles:Amortized intangibles:Amortized intangibles:
Core technologyCore technology19 years$134.5 $(83.0)$51.5 Core technology19 years$140 $(94)$46 
Customer relationshipsCustomer relationships14 years1,021.3 (248.0)773.3 Customer relationships14 years1,024 (306)718 
Product relationshipsProduct relationships11 years270.4 (217.5)52.9 Product relationships11 years281 (237)44 
OtherOther5 years15.5 (4.5)11.0 Other5 years17 (8)
Total intangible assets$1,441.7 $(553.0)$888.7 
Total other intangiblesTotal other intangibles$1,462 $(645)$817 
Amortization expense related to definite-lived long-livedother intangible assets was $23.0$34 million and $46.0$57 million for the three and six months ended December 31, 2021, respectively, and $23 million and $46 million for the three and six months ended December 31, 2020, respectively, and $21.8 million and $43.3 million for the three and six months ended December 31, 2019, respectively.
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Future amortization expense related to definite-lived long-livedother intangible assets for the next five fiscal years is estimated to be:
(Dollars in millions)(Dollars in millions)Remainder 
Fiscal 2021
20222023202420252026(Dollars in millions)Remainder 
Fiscal 2022
20232024202520262027
Amortization expenseAmortization expense$46.6 $92.5 $91.7 $90.6 $89.6 $82.1 Amortization expense$66 $132 $132 $129 $122 $105 

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6.    LONG-TERM OBLIGATIONS AND SHORT-TERM BORROWINGS
Long-term obligations and short-term borrowings consisted of the following at December 31, 20202021 and June 30, 2020:2021:
(Dollars in millions)MaturityDecember 31, 2020June 30,
2020
Senior secured credit facilities
U.S. dollar-denominated term loan facilityMay 2026$924.6 $928.5 
U.S. dollar-denominated 4.875% senior notes due 2026January 2026445.8 445.4 
U.S. dollar-denominated 5.00% senior notes due 2027July 2027493.6 493.1 
Euro-denominated 2.375% senior notes due 2028(1)
March 2028993.1 909.9 
Deferred purchase considerationOctober 202148.7 97.5 
Finance lease obligations2020 to 2044147.3 142.2 
Other obligations2020 to 20242.7 1.4 
Total$3,055.8 $3,018.0 
Less: current portion of long-term obligations and other short-term
borrowings
72.0 72.9 
Long-term obligations, less current portion$2,983.8 $2,945.1 
(Dollars in millions)MaturityDecember 31, 2021June 30,
2021
Senior secured credit facilities
Term loan facility B-3February 2028$1,440 $997 
5.000% senior notes due 2027July 2027500 500 
2.375% euro senior notes due 2028(1)
March 2028933 984 
3.125% senior notes due 2029February 2029550 550 
3.500% senior notes due 2030April 2030650 ��� 
Deferred purchase consideration— 50 
Financing lease obligations2022 to 2038188 193 
Other obligations2022 to 2028
Unamortized discount and debt issuance costs(44)(36)
Total debt$4,220 $3,241 
Less: current portion of long-term obligations and other short-term
     borrowings
29 75 
Long-term obligations, less current portion$4,191 $3,166 
(1) The increasedecrease in Euro-denominatedeuro-denominated debt iswas primarily due to a large fluctuationfluctuations in foreign currency exchange rates.
Senior Secured Credit Facilities and Sixth Amendment to the Credit Agreement
In September 2021, Operating Company entered into Amendment No. 6 (the "Sixth Amendment") to its Amended and Restated Credit Agreement, dated May 20, 2014 (as subsequently amended, the "Credit Agreement"). Pursuant to the Sixth Amendment, Operating Company incurred an additional $450 million aggregate principal amount of U.S. dollar-denominated term loans (the "Incremental Term B-3 Loans") and amended the quarterly amortization from 0.25% to 0.2506% for the Incremental Term B-3 Loans and all of the remaining U.S. dollar-denominated term loans outstanding (together with the Incremental Term B-3 Loans, the “Term B-3 Loans”). The Incremental Term B-3 Loans otherwise feature the same principal terms as the existing Term B-3 Loans, with an interest rate of one-month LIBOR (subject to a floor of 0.50%) plus 2.00% per annum and a maturity date of February 2028. The proceeds of the Incremental Term B-3 Loans, after payment of the offering fees and expenses, were used in part to fund a portion of the consideration paid at the closing of the Bettera acquisition.
3.500% Senior Notes due 2030
In September 2021, Operating Company completed a private offering of $650 million aggregate principal amount of 3.500% Senior Notes due 2030 (the "2030 Notes"). The 2030 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 2030 Notes were offered in the U.S. to qualified institutional buyers in reliance on Rule 144A under the Securities Act of 1933, as amended (the “Securities Act”) and outside the U.S. only to non-U.S. investors pursuant to Regulation S under the Securities Act. The 2030 Notes will mature on April 1, 2030 and bear interest at the rate of 3.500% per annum payable semi-annually in arrears on April 1 and October 1 of each year, beginning on April 1, 2022. The proceeds of the 2030 Notes, after payment of the offering fees and expenses, were used to fund a portion of the consideration paid at the closing of the Bettera acquisition.
Deferred Purchase Consideration

In connection with the acquisition of Catalent Indiana, LLC in October 2017, $200.0$200 million of the $950.0$950 million aggregate nominal purchase price iswas payable in $50.0$50 million installments on each of the first four anniversaries of the closing date. The Company made the first three installment payments in October 2018, October 2019, and October 2020. The balance of the deferred purchase consideration was recorded at fair value as of the acquisition date, with the difference between the remaining nominal amount2020, and the fair value treated as imputed interest.

final installment payment in October 2021.
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Measurement of the Estimated Fair Value of Debt

The measurement of the estimated fair value of the Company’s senior secured credit facilities and other senior indebtedness is classified as a Level 2 determination (see Note 11, Fair Value Measurements, for a description of the method by which fair value classifications are determined) in the fair-value hierarchy and is calculated by using a discounted cash flow model with thea market interest rate as a significant input. The carrying amounts and the estimated fair values of the Company’s principal categories of debt as of December 31, 20202021 and June 30, 20202021 are as follows:

December 31, 2020June 30, 2020
(Dollars in millions)Fair Value Measurement
Carrying
Value
Estimated Fair
Value
Carrying
Value
Estimated Fair
Value
U.S. dollar-denominated 4.875% senior notes due 2026Level 2445.8 458.6 445.4 463.6 
U.S. dollar-denominated 5.00% senior notes due 2027Level 2493.6 539.2 493.1 537.9 
Euro-denominated 2.375% senior notes due 2028Level 2993.1 1,005.3 909.9 844.1 
Senior secured credit facilities & otherLevel 21,123.3 1,134.3 1,169.6 1,160.1 
Total$3,055.8 $3,137.4 $3,018.0 $3,005.7 

December 31, 2021June 30, 2021
(Dollars in millions)Fair Value Measurement
Carrying
Value
Estimated Fair
Value
Carrying
Value
Estimated Fair
Value
5.000% senior notes due 2027Level 2$500 $531 $500 $539 
2.375% Euro senior notes due 2028Level 2933 936 984 993 
3.125% senior notes due 2029Level 2550 541 550 524 
3.500% senior notes due 2030Level 2650 639 — — 
Senior secured credit facilities & otherLevel 2$1,631 $1,608 $1,243 $1,209 
Subtotal$4,264 $4,255 $3,277 $3,265 
Unamortized discount and debt issuance costs(44)— (36)— 
Total debt$4,220 $4,255 $3,241 $3,265 

7.    EARNINGS PER SHARE

The Company computes earnings per share of the Company’s Common Stockcommon stock, par value $0.01 (the “Common Stock”) using the two-class method required due to the participating nature of the Series A Preferred Stock (as defined and discussed in Note 13,14, Equity, Redeemable Preferred Stock, and Accumulated Other Comprehensive LossLoss). Diluted net 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 Company applies the if-converted method to compute the potentially dilutive effect of the Series A Preferred Stock. The reconciliations between basic and diluted earnings per share attributable to Catalent common shareholders for the three and six months ended December 31, 20202021 and 2019,2020, respectively, are as follows (in millions, except share and per share data):follows:

Three Months Ended  
December 31,
Six Months Ended  
December 31,
Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)2020201920202019
(In millions except per share data)(In millions except per share data)2021202020212020
Net earningsNet earnings$88.4 $45.5 $170.8 $45.6 Net earnings$97 $88 $190 $171 
Less: Net earnings attributable to preferred shareholdersLess: Net earnings attributable to preferred shareholders(11.8)(11.2)(25.4)(18.7)Less: Net earnings attributable to preferred shareholders(4)(11)(13)$(26)
Net earnings attributable to common shareholdersNet earnings attributable to common shareholders$76.6 $34.3 $145.4 $26.9 Net earnings attributable to common shareholders$93 $77 $177 $145 
Weighted average shares outstanding - basicWeighted average shares outstanding - basic167,075,141 146,068,025 165,589,730 145,865,570 Weighted average shares outstanding - basic175 167 173 166 
Weighted average dilutive securities issuable - stock plansWeighted average dilutive securities issuable - stock plans2,203,948 1,622,896 2,498,460 1,904,121 Weighted average dilutive securities issuable - stock plans
Weighted average diluted shares outstanding - diluted169,279,089 147,690,921 168,088,190 147,769,691 
Weighted average shares outstanding - dilutedWeighted average shares outstanding - diluted177 169 175 168 
Earnings per share:Earnings per share: Earnings per share: 
BasicBasic$0.46 $0.23 $0.88 $0.18 Basic$0.53 $0.46 $1.02 $0.88 
DilutedDiluted$0.45 $0.23 $0.87 $0.18 Diluted$0.52 $0.45 $1.01 $0.87 

The Company's Series A Preferred Stock iswas deemed a participating security, meaning that it has the right to participate in undistributed earnings with the Company's Common Stock. On November 23, 2020 (the “Partial Conversion Date”), the holders of Series A Preferred Stock converted 265,233265,223 shares of Series A Preferred Stock and $1.9$2 million of unpaid accrued dividends into shares of Common Stock (the “Partial Conversion”). TheThese holders received 20.33 shares of Common Stock for
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each converted preferred share of Series A Preferred Stock, resulting in the aggregate issuance of 5,392,280 shares of Common Stock.Stock by the Company. On November 18, 2021 (the “Final Conversion Date”), the holders of Series A Preferred Stock converted the remaining 384,777 shares of Series A Preferred Stock and $2 million of unpaid accrued dividends into shares of Common Stock (the “Final Conversion”). These holders received 20.32 shares of Common Stock for each converted share of Series A Preferred Stock, resulting in the aggregate issuance of 7,817,554 shares of Common Stock by the Company. See Note 13,14, Equity, Redeemable Preferred Stock and Accumulated Other Comprehensive Loss for further details. There was no anti-dilutive impact from employee-held stock options and restricted stock units in the computation

The diluted weighted average number of diluted earnings per share for both the three and six months endedshares outstanding as of December 31, 2020. The computation of diluted earnings per share for both2021 did not include the three and six months ended December 31, 2020 excludes the effect of
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approximately 7.7 million “if-converted”following shares of Common Stock potentially issuable onassociated with the conversion of Series A Preferred Stock as thoseor the shares would be anti-dilutive.associated with the following types of outstanding equity grants due to their antidilutive effect:
The computations of diluted earnings per share for the three and six months ended December 31, 2019 exclude the effect of Common Stock potentially issuable under employee-held stock options and restricted stock units of approximately 0.7 million and 1.0 million, respectively, because they are anti-dilutive. Further, the computation of diluted earnings per share for the three and six months ended December 31, 2019, respectively, excludes the effect of approximately 13.1 million “if-converted” shares of Common Stock potentially issuable on the conversion of Series A Preferred Stock, as those shares would be anti-dilutive.
Three Months Ended  
December 31,
Six Months Ended 
December 31,
(share counts in millions)2021202020212020
Stock options— — — — 
Time-based restricted stock units— — — — 
Performance-based restricted stock units— — — — 
Series A Preferred Stock— — 
8.    OTHER EXPENSE (INCOME) EXPENSE,, NET
The components of other expense (income) expense,, net for the three and six months ended December 31, 20202021 and 20192020 are as follows:
Three Months Ended  
December 31,
Six Months Ended 
December 31,
(Dollars in millions)2020201920202019
Other (income) expense, net
Debt refinancing costs$— $— $— $0.1 
Foreign currency (gains) losses (1)
(0.2)6.7 (0.8)3.6 
     Other (2)
(8.1)(11.1)(18.7)(3.2)
Total other (income) expense, net$(8.3)$(4.4)$(19.5)$0.5 
Three Months Ended  
December 31,
Six Months Ended 
December 31,
(Dollars in millions)2021202020212020
Debt financing costs (1)
$— $— $$— 
Foreign currency losses (gains) (2)
15 — 24 (1)
     Other (3)
(1)(8)(5)(18)
Total other expense (income), net$14 $(8)$23 $(19)

(1) Debt financing costs for the six months ended December 31, 2021 includes $4 million of financing charges related to the Company’s Incremental Term B-3 Loans.
(2) Foreign currency remeasurement gainslosses (gains) include both cash and non-cash transactions.

(2)(3) Other, for the three and six months ended December 31, 20202021, includes total realized and unrealizeda gain of $7.0$2 million and $16.0 million, respectively, related to the fair value of the derivative liability associated with the Series A Preferred Stock. Other, for the three and six months ended December 31, 20192020, includes a total unrealized gain of $10.3$7 million and $1.4 $16 million, respectively, related to the fair value of the derivative liability associated with the Series A Preferred Stock.
9.     RESTRUCTURING AND OTHER COSTS
From time to time, the Company has implemented plans to restructure certain operations, both domestically and internationally. The restructuring plans focused on various aspects of operations, including 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 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 costs consist of accelerated depreciation, equipment relocation costs and costs associated with planned facility expansions and closures to streamline Company operations.
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During the three monthsfiscal year ended December 31, 2020,June 30, 2021, the Company adopted a plan to reduce costs and optimize its infrastructure in Western Europe by closing its Clinical Supply Services facility in Bolton, United Kingdom (“U.K.”) In connection with this restructuring plan, the Company expects to reducereduced its headcount between 150 andby approximately 180 employees through December 31, 2021 and estimates that it will incurincurred cumulative charges between $4.0 million and $7.0of $8 million, primarily associated with employee severance benefits.
For both the three months and six months ended December 31, 2020,2021, restructuring charges associated with the Bolton facility closure were $4.0 million.$1 million and $2 million, respectively.
Total restructuring charges, inclusive of the charges associated with the Bolton facility closure, were $1 million and $5 million for the three months ended December 31, 2021 and 2020, and 2019respectively. Total restructuring charges, inclusive of the charges associated with the Bolton facility closure, were $5.5$2 million and $0.5$6 million respectively, and for the six months ended December 31, 20202021 and 2019 were $6.4 million and $1.2 million,2020, respectively.

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10.    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 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, 2020,2021, the Company had euro-denominated debt outstanding of $993.1$933 million (U.S. dollar equivalent) that, 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 portion of translation gains or losses are reported in accumulated other comprehensive loss as part of the cumulative translation adjustment. The non-hedge portions of the euro-denominated debt translation gains or losses are reported in the consolidated statement of operations. The following table includes net investment hedge activity during the three and six months ended December 31, 20202021 and 2019.2020.
Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)2020201920202019
Unrealized foreign exchange gain (loss) within other
     comprehensive income
$(45.4)$(6.5)$(77.8)$13.8 
Unrealized foreign exchange gain (loss) within statement
     of operations
$(2.5)$(3.9)$(4.4)$(5.8)
Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)2021202020212020
Unrealized foreign exchange gain (loss) within other comprehensive income$40 $(45)$62 $(78)
Unrealized foreign exchange loss within statement of operations$(8)$(3)$(11)$(4)
The net accumulated lossgain on the instrument designated as a hedge as of December 31, 20202021 within other comprehensive income (loss)loss was approximately $15.3$68 million. Amounts are reclassified out of accumulated other comprehensive loss into earnings when the entity to which the gains and losses relate is either sold or substantially liquidated.
Preferred Stock Derivative Liability
As discussed in Note 13,14, Equity, Redeemable Preferred Stock, and Accumulated Other Comprehensive Loss, in May 2019, the Company issued shares of Series A Preferred Stock in exchange for net proceeds of $646.3$646 million after taking into account the $3.7$4 million issuance cost.
The dividend rate used to determine the amount of the quarterly dividend payable on shares of the Series A Preferred Stock iswas subject to adjustment so as to provide holders of shares of Series A Preferred Stock with certain protections against a decline in the trading price of shares of Common Stock. The Company determined that this feature should be accounted for as a derivative liability, since the feature fluctuates inversely to changes in the trading price and is also linked to the performance of the S&P 500 stock index. Accordingly, the Company bifurcated the adjustable dividend feature from the remainder of the Series A Preferred Stock and accounted for this feature as a derivative liability at fair value. The Company will recognize changes in the fair value of the derivative liability in the consolidated statements of operations for each reporting period. The fair value was determined using an option pricing methodology, specifically both a Monte Carlo simulation and a binomial lattice model. The methodology incorporates the terms and conditions of the preferred stock arrangement, historical stock price volatility, the risk-free interest rate, a credit spread based on the yield indexes of high-yield bonds, and the trading price of shares of the Common Stock. The calculation of the estimated fair value of the derivative liability is highly sensitive to changes in unobservable inputs, such as the expected volatility and the Company’s specific credit spread.
The Company recorded a total gain of $7.0$0 million and $7 million on the change in the estimated fair value of the derivative liability for the three months ended December 31, 2021 and 2020, primarily related to volatility in the price of the Company’s Common Stock that is used to estimate the fair value,respectively, which is reflected as Otherother expense (income) expense,, net in the consolidated statements of operations.
A portion of the derivative liability was settled on the Partial Conversion Date due to the Partial Conversion. The fair value of the derivative liability as of the Partial Conversion Date was $8.6$9 million, of which $3.5$4 million was related to the converted portion of the outstanding shares of Series A Preferred Stock. The remainder of the derivative liability was settled on the Final Conversion Date due to the Final Conversion. The fair value of the derivative liability as of the Final Conversion Date
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was $1 million. See Note 13,14, Equity, Redeemable Preferred Stock, and Accumulated Other Comprehensive Loss for details of the Partial and Final Conversion.
The fair value of the derivative liability that relates to outstanding shares of Series A Preferred Stock as of December 31, 2020 was $4.1 million.
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The fair value is classified as Level 3 in the fair-value hierarchy due to the significant management judgment required for the assumptions underlying the calculation of value. The following table sets forth a summary of changes in the estimated fair value of the derivative liability:
(Dollars in millions)Fair Value Measurements of
Series A Preferred Stock
Derivative Liability
Using Significant
Unobservable Inputs (Level 3)
Balance at June 30, 2020$23.6 
Change in estimated fair value of Series A Preferred Stock derivative liability(16.0)
Settlement of derivative liability upon Partial Conversion(3.5)
Balance at December 31, 2020$4.1 

Interest-Rate Swap
PursuantIn April 2020, pursuant to its interest rate and risk management strategy, in April 2020, Operatingthe Company entered into an interest-rate swap agreement with Bank of America N.A. (the “2020 Rate Swap”) as a hedge against the economic effect of a portion of the variable interest obligation associated with its U.SU.S. dollar-denominated term loans under its senior secured credit facilities, so thatfacilities. The 2020 Rate Swap effectively fixed the rate of interest payable on that portion of the debt, becomesthereby reducing the impact of future interest rate changes on future interest expense.
In February 2021, in connection with an amendment to the Credit Agreement, the Company paid $2 million in cash to Bank of America N.A to settle the 2020 Rate Swap. This loss is deferred in stockholders’ equity, net of income taxes, as a component of accumulated other comprehensive loss, and amortized as an adjustment to interest expense, net over the original term of the formerly outstanding term loans. The net amount of deferred losses on cash flow hedges that is expected to be reclassified from accumulated other comprehensive loss into interest expense, net within the next twelve months is not material.
In February 2021, the Company entered into a new interest-rate swap agreement with Bank of America N.A. (the “2021 Rate Swap”) as a hedge against the economic effect of a portion of the variable interest obligation associated with its Term B-3 Loans. The 2021 Rate Swap effectively fixed at a certainthe rate of interest payable on that portion of the Term B-3 Loans, thereby reducing the impact of future interest rate changes on future interest expense. As a result of entering into the interest-rate swap agreement,2021 Rate Swap, the floatingvariable portion of the applicable interest rate on $500.0$500 million of the term loansTerm B-3 Loans is now effectively fixed at 1.26%, for a total fixed rate of 3.51%0.9985%.
The interest-rate swap agreement2021 Rate Swap qualifies for and is designated as a cash-flow hedge. The Company evaluates hedge effectiveness at the inception of the hedge and on an ongoing basis. The cash flows associated with the 2021 Rate Swap is reported in cash provided by operating activities in the consolidated statements of cash flows. The unrealized gain or loss from marking the 2021 Rate Swap to market during the three and six months ended December 31, 2021 was immaterial in each period.
A summary of the estimated fair value of the 2021 Rate Swap reported in the consolidated balance sheets is stated in the table below:
December 31, 2021June 30, 2021
(Dollars in millions)Balance Sheet ClassificationEstimated Fair ValueBalance Sheet ClassificationEstimated Fair Value
Interest-rate swapOther long-term assets$Other long-term assets$

11. FAIR VALUE MEASUREMENTS
ASC 820, Fair Value Measurement, defines fair value as the exit price that would be received to sell an asset or paid to transfer a liability. Fair value is a market-based measurement that should be determined using assumptions that market participants would use in pricing an asset or liability. Valuation techniques used to measure fair value should maximize the use of observable inputs and 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 Level 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 fair value of the 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.
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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, 2021 and June 30, 2021, respectively:

(Dollars in millions)Basis of Fair Value Measurement
December 31, 2021TotalLevel 1Level 2Level 3
Assets:
Marketable securities$66 $66 $— $— 
Interest-rate swap— — 
Trading securities— — 
June 30, 2021
Assets:
Marketable securities$71 $71 $— $— 
Interest-rate swap— — 
Trading securities— — 
Liabilities:
Series A Preferred Stock derivative liability— — 
The fair value of the interest-rate swap agreement2021 Rate Swap is determined at the end of each reporting period based on valuation models that use interest rate yield curves and discount rates as inputs. The discount rates are based on U.S. deposit or U.S. Treasury rates. The significant inputs used in the valuation models are readily available in public markets or can be derived from observable market transactions, and therefore, the valuation has beenis therefore classified as a Level 2 in the fair-value hierarchy.
The estimated fair value of the Series A Preferred Stock derivative was determined using an option pricing methodology, specifically both a Monte Carlo simulation and a binomial lattice model. The methodology incorporated the terms and conditions of the preferred stock arrangement, historical stock price volatility, the risk-free interest rate, swapa credit spread based on the yield indexes of high-yield bonds, and the trading price of shares of     Common Stock. The calculation of the estimated fair value of the derivative liability was highly sensitive to changes in unobservable inputs, such as the expected volatility and the Company’s credit spread. The estimated fair value of boththe Series A Preferred Stock derivative liability was classified as Level 3 in the fair-value hierarchy due to the significant management judgment required to make the assumptions underlying the calculation of value.
The following table sets forth a summary of changes in the estimated fair value of the Series A Preferred Stock derivative liability from June 30, 2021 to December 31, 20202021:
(Dollars in millions)Fair Value Measurements of
Series A Preferred Stock
Derivative Liability
Using Significant
Unobservable Inputs (Level 3)
Balance at June 30, 2021$
Change in estimated fair value of Series A Preferred Stock derivative liability(2)
Settlement of derivative liability upon Final Conversion(1)
Balance at December 31, 2021$— 

Assets and asLiabilities Measured at Fair Value on a Non-Recurring Basis
Long-lived assets, goodwill, and other intangible assets are subject to non-recurring fair value measurement for the evaluation of June 30, 2020potential impairment. Other than the fair value estimates disclosed in Note 3, Business Combinations and Divestitures, there was reported as a derivative liability of $3.7 million within other liabilities in the consolidated balance sheets. The cash flows associated with the interest-rate swap are reported in net cash provided by operating activities in the consolidated statements of cash flows. The unrealized gain or loss from the mark-to-market of the interest rate swap valuationno non-recurring fair value measurement during the six months ended December 31, 20202021 and the fiscal year ended June 30, 2020 was immaterial in each period.2020.
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11.12.    INCOME TAXES

The Company accounts for income taxes in accordance with ASC 740, Income Taxes. Generally, fluctuations in the effective tax rate are due to changes in relative amounts of U.S. and non-U.S. pretax income, the tax impact of special items, and other discrete tax items. 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 certain equity compensation.
In the normal course of business, the Company is subject to examination by taxing authorities around the world, including such major jurisdictions as the United States,U.S., Germany, and the United Kingdom.U.K. The Company is no longer subject to examinations by theany relevant tax authoritiesauthority for years prior to fiscal year 2009. The Company is presently under audit in select jurisdictions in the United States and in Europe, but no material impact is expected to the financial results once these audits are completed.

ASC 740 includesprovides guidance onfor the accounting forof uncertain income tax positions recognized in ourthe 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, 20202021 and June 30, 2020,2021, the Company had an aggregate of $4.1 million and $5.6 million, respectively, of reservesCompany's reserve against uncertain income tax positions (including accrued interest and penalties). As of these dates, $3.2 million and $4.4 million, respectively, represent the amount of unrecognized tax benefits, which, if recognized, would favorably affect the effective income tax rate. The reduction to unrecognized tax benefits is primarily driven by a settlement of an income tax audit that occurred in the fiscal quarter that ended September 30, 2020.remained substantially unchanged at approximately $5 million. Interest and penalties related to uncertain tax positions are recognized as a component of income tax expense.
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The Company recorded a provision for income taxes for the three months ended December 31, 2021 of $18 million relative to earnings before income taxes of $115 million. The Company recorded a provision for income taxes for the three months ended December 31, 2020 of $20.6$21 million relative to earnings before income taxes of $109.0$109 million. The Company recorded a provision for income taxes for the three months ended December 31, 2019 of $13.0 million relative to earnings before income taxes of $58.5 million. The increaseddecrease in income tax provision forrelative to the currentprior-year period was largely impacted by an increasethe result of a shift in pretax income across severalin international tax jurisdictions and partially offset by an increase in discrete benefit items including certain equity compensation deductions.with favorable tax rates. Generally, fluctuations in the effective tax rate are due to changes in the geographic distribution of our pretax income 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 recorded a provision for income taxes for the six months ended December 31, 2021 of $28 million relative to earnings before income taxes of $218 million. The Company recorded a provision for income taxes for the six months ended December 31, 2020 of $5.6$5 million relative to earnings before income taxes of $176.4$176 million. The Company recordedincrease in the provision relative to the prior-year period was the result of a decrease in non-U.S. tax credits claimed on an amended U.S. federal income tax filing compared to the prior-year period. The provision for income taxes forin each of these periods was also impacted by the six months ended December 31, 2019relative amount and mix of $6.1 million relative to earnings before income taxes of $51.7 million. The reducedpermanent tax adjustments included in the income tax provision for the current six-month period reflects a $22.2 million benefit for U.S. foreign tax credits resulting from an amendment to a prior-year return. Generally, fluctuations in the effective tax rate are due to changes in the geographic distribution of the Company's pretax income, the tax impact of permanent differences, restructuring, special items, certain equity related compensation,computation and other discrete tax items that may have unique tax implications depending onrecognized in the nature of the item.periods.
12.13.    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,
Six Months Ended  
December 31,
(Dollars in millions)(Dollars in millions)2020201920202019(Dollars in millions)2021202020212020
Components of net periodic benefit cost:Components of net periodic benefit cost:Components of net periodic benefit cost:
Selling, general, and administrative expenses:Selling, general, and administrative expenses:Selling, general, and administrative expenses:
Service costService cost$1.0 $0.8 $2.0 $1.4 Service cost$$$$
Other (income) expense, net:
Other expense (income), net:Other expense (income), net:
Interest costInterest cost1.1 1.8 2.1 3.5 Interest cost
Expected return on plan assetsExpected return on plan assets(2.5)(2.6)(4.9)(5.3)Expected return on plan assets(3)(2)(5)(5)
Amortization (1)
Amortization (1)
0.8 0.7 1.4 1.5 
Amortization (1)
— 
Net amount recognizedNet amount recognized$0.4 $0.7 $0.6 $1.1 Net amount recognized$— $— $$
(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. The liability reported reflects the present value of the Company’s expected future long-term obligations. The estimated discounted value of the projected contributions related to such plans was $38.6$38 million as of December 31, 20202021 and June 30, 2020,
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2021, and is included within pension liability on the consolidated balance sheets. The annual cash impact associated with the Company’s obligations in such plan is approximately $1.7 million per year.

$2 million.    
13.14.    EQUITY, REDEEMABLE PREFERRED STOCK, AND ACCUMULATED OTHER COMPREHENSIVE LOSS
Description of Capital Stock
The Company is authorized to issue 1,000,000,0001.00 billion shares of its Common Stock and 100,000,000100 million shares of preferred stock, par value $0.01 per share. In accordance with the Company’s amended and restated certificate of incorporation, each share of Common Stock has one vote, and the Common Stock votes together as a single class.
Recent Public Offerings of its Common Stock
On June 15, 2020, the Company completed a public offering of its Common Stock (the “June 2020 Equity Offering”), in which the Company sold 7.7 million shares of Common Stock at a price of $70.72 per share, net of underwriting discounts and commissions. The Company obtained total net proceeds from the June 2020 Equity Offering of $547.5 million after the payment of associated offering expenses. The net proceeds of the June 2020 Equity Offering were used to repay $200.0 million
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of precautionary borrowings from the third quarter of fiscal 2020 under Operating Company's revolving credit facility, with the remainder available for general corporate purposes. On July 10, 2020, the underwriter for the June 2020 Equity Offering exercised its over-allotment option on 1.2 million additional shares, resulting in supplemental net proceeds of $81.8 million from the June 2020 Equity Offering, which was recorded in the current period.
On February 6, 2020, the Company completed the February 2020 Equity Offering, in which the Company sold 8.4 million shares of Common Stock at a price of $58.58 per share, net of underwriting discounts and commissions. The Company obtained total net proceeds from the February 2020 Equity Offering of $494.2 million. The net proceeds of the February 2020 Equity Offering were used to repay $100.0 million of borrowings earlier in the quarter under Operating Company's revolving credit facility and pay the consideration for the MaSTherCell acquisition due at its closing, with the remainder available for general corporate purposes.

Effect of Restricted Stock
Shares of Common Stock outstanding include shares of unvested restricted stock. Unvested restricted stock included in reportable shares outstanding was 0.2 million shares as of December 31, 2020. Shares of unvested restricted stock are excluded from the calculation of basic weighted average shares outstanding, but their dilutive impact is added back in the calculation of diluted weighted average shares outstanding, except when the effect would be anti-dilutive.
Redeemable Preferred Stock
In May 2019, the Company designated 1,000,0001 million shares of its preferred stock, par value $0.01, as its Series A Convertible Preferred Stock (the “Series A Preferred Stock”), pursuant to a certificate of designation of preferences, rights, and limitations (as amended, the “Certificate of Designation”) filed with the Delaware Secretary of State, and issued and sold 650,000 shares of the Series A Preferred Stock for an aggregate purchase price of $650.0$650 million, to affiliates of Leonard Green & Partners, L.P., each share having an initial stated value of $1,000 (as such value may be adjusted in accordance with the terms of the Certificate of Designation). The Series A Preferred Stock ranksranked senior to the Company’s Common Stock with respect to dividend rights and rights upon the voluntary or involuntary liquidation, dissolution, or winding up of the affairs of the Company.
Proceeds from the offering of the Series A Preferred Stock, net of stock issuance costs, were $646.3$646 million, $39.7$40 million of which was allocated to the dividend-adjustment feature at its issuance and separately accounted for as a derivative liability. Any change in the fair value of derivative liability during a fiscal quarter is recorded as a non-operating expense in the consolidated statement of operations. See Note 10, Derivative Instruments and Hedging Activities, for detail concerning the change in fair value during the three and six months ended December 31, 2020.
As described in Note 7, Earnings Per Share, on the Partial Conversion Date, holders of Series A Preferred Stock converted 265,233265,223 shares (approximately 41% of their holdings) and $1.9$2 million of unpaid accrued dividends into shares of Common Stock. TheThese holders received 20.33 shares of Common Stock for each converted preferred share of Series A Preferred Stock, resulting in the issuance of 5,392,280 shares of Common Stock.Stock by the Company. There was no gain or loss recognized upon the Partial Conversion as it occurred in accordance with the original terms of the Certificate of Designation. The Company has 384,777 shares of Series A Preferred Stock that remain outstanding at December 31, 2020.

As a result of the Partial Conversion, additional paid in capital increased $252.9$253 million, which includes $3.5$4 million related to the fair value of the portion of the derivative liability that was settled upon the Partial Conversion and $1.9$2 million related to an unpaid accrued dividend.

On the Final Conversion Date, holders of Series A Preferred Stock converted the remaining 384,777 shares and $2 million of unpaid accrued dividends into shares of Common Stock. These holders received 20.32 shares of Common Stock for each converted share of Series A Preferred Stock, resulting in the issuance of 7,817,554 shares of Common Stock by the Company. There was no gain or loss recognized upon the Final Conversion as it occurred in accordance with the terms of the Certificate of Designation. See Note 10, Derivative Instruments and Hedging Activities, for detail concerning the change in fair value of the derivative during the threesix months ended December 31, 2020.2021.

As a result of the Final Conversion, additional paid in capital increased $362 million, which includes $1 million related to the fair value of the portion of the derivative liability that was settled upon the Final Conversion and $2 million related to an unpaid accrued dividend.

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the Series A Preferred Stock remains outstanding, and the Company has re-assigned all of the authorized shares of Series A Preferred Stock as undesignated shares of preferred stock, par value $0.01.
Accumulated Other Comprehensive Loss
The components of the changes in the cumulative translation adjustment, derivatives and hedges, and minimum pension liability, and marketable securities for the three and six months ended December 31, 20202021 and 20192020 are presented below.
Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)2020201920202019
Foreign currency translation adjustments:
Net investment hedge$(45.4)$(6.5)$(77.8)$13.8 
Long-term intercompany loans16.5 18.1 22.8 11.6 
Translation adjustments58.9 10.2 94.3 (22.0)
Total foreign currency translation adjustment, pretax30.0 21.8 39.3 3.4 
Tax (benefit) expense(9.4)(0.3)(16.0)3.1 
Total foreign currency translation adjustment, net of tax$39.4 $22.1 $55.3 $0.3 
Net change in derivatives and hedges:
Net gain recognized during the period$0.6 $$0.5 $
Total derivatives and hedges, pretax0.6 0.5 
Tax expense0.1 0.1 
Net change in derivatives and hedges, net of tax$0.5 $$0.4 $
Net change in minimum pension liability:
Net gain recognized during the period$0.7 $3.6 $1.4 $2.9 
Total pension liability, pretax0.7 3.6 1.4 2.9 
Tax expense (benefit)0.2 0.3 0.4 (0.1)
Net change in minimum pension liability, net of tax$0.5 $3.3 $1.0 $3.0 
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Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)2021202020212020
Foreign currency translation adjustments:
Net investment hedge$40 $(45)$62 $(78)
Long-term intercompany loans(4)16 (7)23 
Translation adjustments(45)59 (73)94 
Total foreign currency translation adjustment, pretax(9)30 (18)39 
Tax expense (benefit)(9)14 (16)
Total foreign currency translation adjustment, net of tax$(18)$39 $(32)$55 
Net change in derivatives and hedges:
Net gain recognized during the period$$— $$
Total derivatives and hedges, pretax— 
Tax expense— — 
Net change in derivatives and hedges, net of tax$$— $$
Net change in minimum pension liability:
Net gain recognized during the period$— $$$
Total pension liability, pretax— 
Tax benefit— — — — 
Net change in minimum pension liability, net of tax$— $$$
Net change in marketable securities:
Net loss recognized during the period$(1)$— $(1)$— 
Total available for sale investment, pretax(1)— (1)— 
Tax benefit— — — — 
Net change in marketable securities, net of tax$(1)$— $(1)$— 
For the three months ended December 31, 2020,2021, 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 September 30, 2020$(319.2)$(47.0)$(2.7)$(1.1)$(370.0)
Other comprehensive income before
reclassifications
39.4 0.5 39.9 
Amounts reclassified from accumulated other
comprehensive loss
0.5 0.5 
Net current period other comprehensive income39.4 0.5 0.5 40.4 
Balance at December 31, 2020$(279.8)$(46.5)$(2.2)$(1.1)$(329.6)
(Dollars in millions)Foreign Exchange Translation AdjustmentsPension and Liability AdjustmentsDerivatives and HedgesMarketable SecuritiesOtherTotal
Balance at September 30, 2021$(282)$(46)$$(1)$(1)$(329)
Other comprehensive (loss) income before
    reclassifications
(18)— (1)— (16)
Amounts reclassified from accumulated other
    comprehensive loss
— — — — — — 
Net current period other comprehensive (loss)
    income
(18)— (1)— (16)
Balance at December 31, 2021$(300)$(46)$$(2)$(1)$(345)
For the six months ended December 31, 2020,2021, the changes in accumulated other comprehensive loss, net of tax by component are as follows:
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(Dollars in millions)Foreign Exchange Translation AdjustmentsPension and Liability AdjustmentsDerivatives and HedgesOtherTotal
Balance at June 30, 2020$(335.1)$(47.5)$(2.6)$(1.1)$(386.3)
Other comprehensive income before
reclassifications
55.3 0.4 55.7 
Amounts reclassified from accumulated other
comprehensive loss
1.0 1.0 
Net current period other comprehensive income55.3 1.0 0.4 56.7 
Balance at December 31, 2020$(279.8)$(46.5)$(2.2)$(1.1)$(329.6)

(Dollars in millions)Foreign Exchange Translation AdjustmentsPension and Liability AdjustmentsDerivatives and HedgesMarketable SecuritiesOtherTotal
Balance at June 30, 2021$(268)$(47)$— $(1)$(1)$(317)
Other comprehensive (loss) income before
    reclassifications
(32)— (1)— (29)
Amounts reclassified from accumulated other
    comprehensive loss
— — — — 
Net current period other comprehensive (loss)
    income
(32)(1)— (28)
Balance at December 31, 2021$(300)$(46)$$(2)$(1)$(345)
14.15.    COMMITMENTS AND CONTINGENCIES
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 consolidated 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.

15.16.    SEGMENT INFORMATION
The Company conducts its business within the following operating segments: Biologics, Softgel and Oral Technologies, Oral and Specialty Delivery, and Clinical Supply Services. The Company evaluates the performance of its segments based on segment earnings before other (expense) income, impairments, restructuring costs, interest expense, income tax expense (benefit), and depreciation and amortization ((“Segment EBITDAEBITDA”).EBITDA from operations is consolidated earnings from operations before interest expense, income tax expense (benefit), and depreciation and amortization.
Segment EBITDA and
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Tableis subject to important limitations. These consolidated financial statements include information concerning Segment EBITDA (a) because Segment EBITDA is an operational measure used by management in the assessment of Contents
EBITDA from operations are not definedthe operating segments, the allocation of resources to the segments, and the setting of strategic goals and annual goals for the segments, and (b) in U.S. GAAP andorder to provide supplemental information that the Company considers relevant for the readers of the consolidated financial statements. The Company’s presentation of Segment EBITDA may not be comparable to similarly titled measures used by other companies.
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The following tables include net revenue and Segment EBITDA for each of the Company's current reporting segments during the three and six months ended December 31, 20202021 and 2019:2020:
(Dollars in millions)(Dollars in millions)Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)Three Months Ended  
December 31,
Six Months Ended  
December 31,
20202019202020192021202020212020
Net revenue:Net revenue:Net revenue:
BiologicsBiologics$403.9 $225.2 $781.0 $413.8 Biologics$638 $404 $1,184 $781 
Softgel and Oral TechnologiesSoftgel and Oral Technologies246.6 267.9 $467.7 $528.5 Softgel and Oral Technologies329 247 572 468 
Oral and Specialty DeliveryOral and Specialty Delivery169.9 143.2 328.2 275.8 Oral and Specialty Delivery156 170 302 328 
Clinical Supply ServicesClinical Supply Services93.5 87.9 186.2 172.5 Clinical Supply Services99 93 195 186 
Inter-segment revenue eliminationInter-segment revenue elimination(3.1)(2.8)(6.6)(4.5)Inter-segment revenue elimination(5)(3)(11)(6)
Total net revenueTotal net revenue$910.8 $721.4 $1,756.5 $1,386.1 Total net revenue$1,217 $911 $2,242 $1,757 
(Dollars in millions)(Dollars in millions)Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)Three Months Ended  
December 31,
Six Months Ended  
December 31,
20202019202020192021202020212020
Segment EBITDA reconciled to net earnings:Segment EBITDA reconciled to net earnings:Segment EBITDA reconciled to net earnings:
BiologicsBiologics$135.5 $63.0 $242.0 $98.8 Biologics$197 $136 $363 $242 
Softgel and Oral TechnologiesSoftgel and Oral Technologies45.6 64.5 $83.4 $110.9 Softgel and Oral Technologies78 46 119 83 
Oral and Specialty DeliveryOral and Specialty Delivery44.2 33.1 65.6 60.8 Oral and Specialty Delivery44 44 77 66 
Clinical Supply ServicesClinical Supply Services25.3 24.0 50.3 45.6 Clinical Supply Services27 25 53 50 
Sub-TotalSub-Total$250.6 $184.6 $441.3 $316.1 Sub-Total$346 $251 $612 $441 
Reconciling items to net earningsReconciling items to net earningsReconciling items to net earnings
Unallocated costs (1)
Unallocated costs (1)
(44.7)(29.3)(73.6)(70.7)
Unallocated costs (1)
(101)(45)(157)(74)
Depreciation and amortizationDepreciation and amortization(71.0)(61.9)(140.1)(122.5)Depreciation and amortization(98)(71)(179)(140)
Interest expense, netInterest expense, net(25.9)(34.9)(51.2)(71.2)Interest expense, net(32)(26)(58)(51)
Income tax expenseIncome tax expense(20.6)(13.0)$(5.6)(6.1)Income tax expense(18)(21)(28)(5)
Net earningsNet earnings$88.4 $45.5 $170.8 $45.6 Net earnings$97 $88 $190 $171 
(1) Unallocated costs include restructuring and special items, stock-based compensation, gain on sale of subsidiary, impairment charges, certain other corporate directed costs, and other costs that are not allocated to the segments as follows:
Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)(Dollars in millions)Three Months Ended  
December 31,
Six Months Ended  
December 31,
(Dollars in millions)20202019202020192021202020212020
Impairment charges and gain (loss) on sale of assets(a)Impairment charges and gain (loss) on sale of assets(a)$(0.6)$(1.7)$(2.4)$(1.5)Impairment charges and gain (loss) on sale of assets(a)$(16)$(1)$(19)$(2)
Stock-based compensationStock-based compensation(11.4)(10.3)(30.1)(26.9)Stock-based compensation(11)(11)(32)(30)
Restructuring and other special items (a)(b)
Restructuring and other special items (a)(b)
(14.7)(7.9)(19.6)(19.7)
Restructuring and other special items (a)(b)
(23)(15)(31)(20)
Gain on sale of subsidiary (c)
Gain on sale of subsidiary (c)
— — — 
Other income (expense), net (b)
8.3 4.4 19.5 (0.5)
Other (expense) income, net (d)
Other (expense) income, net (d)
(14)(23)19 
Unallocated corporate costs, netUnallocated corporate costs, net(26.3)(13.8)(41.0)(22.1)Unallocated corporate costs, net(37)(26)(53)(41)
Total unallocated costsTotal unallocated costs$(44.7)$(29.3)$(73.6)$(70.7)Total unallocated costs$(101)$(45)$(157)$(74)

(a)    Impairment charges and gain (loss) on sale of assets during the three and six months ended December 31, 2021 include fixed asset impairment charges associated with a product in our respiratory and specialty platform.
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(a)(b)    Restructuring and other special items forduring the three months ended December 31, 20202021 include (i) transaction and integration costs forprimarily associated with the sale of the Company's Blow-Fill-Seal BusinessBettera acquisition and (ii) restructuring costs associated with the closure of the Company's Clinical Supply Services facility in Bolton U.K.facility. Restructuring and other special items forduring the six months ended December 31, 2021 include (i) transaction and integration costs associated with the Delphi, Hepatic, RheinCell, and Bettera acquisitions and (ii) restructuring costs associated with the closure of the Bolton facility.
Restructuring and other special items during the three and six months ended December 31, 2020 include (i) transaction costs associated with the sale of the Blow-Fill-Seal Business and (ii) restructuring costs associated with the closure of the Bolton facility. Restructuring and other special items during the six months ended December 31, 2020 also include transaction and integration costs associated with the Anagni, MaSTherCellacquisitions of facilities in Italy and Skeletal acquisitions andBelgium, the disposal of a facilitysite in Australia. RestructuringAustralia, and other special items duringrestructuring initiatives across the three andCompany's network of sites.
(c)    Gain on sale of subsidiary for the six months ended December 31, 2019 include transaction and integration costs associated with2021 was due to the Company’s cell and gene therapy acquisitions andsale of the disposal of a facility in Australia.Blow-Fill-Seal Business.
(b)(d)    Refer to Note 8, Other (income) expense, netExpense (Income), Net for details of financing charges and foreign currency translation adjustments recorded within other income (expense)expense (income), net.

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.
(Dollars in millions)(Dollars in millions)December 31,
2020
June 30,
2020
(Dollars in millions)December 31,
2021
June 30,
2021
Assets:Assets:Assets:
BiologicsBiologics$4,303.5 $3,775.0 Biologics$5,208 $4,973 
Softgel and Oral TechnologiesSoftgel and Oral Technologies1,547.0 1,501.8 Softgel and Oral Technologies2,591 1,604 
Oral and Specialty DeliveryOral and Specialty Delivery1,265.7 1,247.4 Oral and Specialty Delivery1,210 1,269 
Clinical Supply ServicesClinical Supply Services472.2 451.2 Clinical Supply Services465 483 
Corporate and eliminationsCorporate and eliminations609.7 801.1 Corporate and eliminations729 783 
Total assetsTotal assets$8,198.1 $7,776.5 Total assets$10,203 $9,112 

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17. SUPPLEMENTAL BALANCE SHEET INFORMATION
Supplemental balance sheet information at December 31, 20202021 and June 30, 20202021 is detailed in the following tables.
Inventories
Work-in-process and inventories include raw materials, labor, and overhead. Total inventories consist of the following:
(Dollars in millions)(Dollars in millions)December 31,
2020
June 30,
2020
(Dollars in millions)December 31,
2021
June 30,
2021
Raw materials and suppliesRaw materials and supplies$338.5 $222.6 Raw materials and supplies$592 $469 
Work-in-processWork-in-process157.0 123.2 Work-in-process153 151 
Total inventories, grossTotal inventories, gross495.5 345.8 Total inventories, gross745 620 
Inventory cost adjustmentInventory cost adjustment(34.2)(22.0)Inventory cost adjustment(57)(57)
Total inventoriesTotal inventories$461.3 $323.8 Total inventories$688 $563 
Prepaid expenses and other
Prepaid expenses and other consist of the following:
(Dollars in millions)December 31,
2020
June 30,
2020
Prepaid expenses$47.5 $28.6 
Contract assets122.9 61.4 
Current assets held for sale (1)
175.1 
Spare parts supplies24.9 23.1 
Prepaid income tax21.5 15.0 
Non-U.S. value-added tax33.4 19.0 
Other current assets27.7 30.8 
Total prepaid expenses and other$453.0 $177.9 
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(Dollars in millions)December 31,
2021
June 30,
2021
Prepaid expenses$54 $46 
Contract assets308 181 
Spare parts supplies21 30 
Prepaid income tax21 22 
Non-U.S. value-added tax35 50 
Other current assets61 47 
Total prepaid expenses and other$500 $376 
(1) Represents current assets associated with the Company's Blow-Fill-Seal Business. See Note 3, Business Combinations and Divestitures for more details.
Property, plant, and equipment, net
Property, plant, and equipment, net consist of the following:
(Dollars in millions)December 31,
2020
June 30,
2020
Land, buildings, and improvements$1,341.3 $1,250.9 
Machinery and equipment1,292.1 1,233.6 
Furniture and fixtures22.4 20.9 
Construction in progress558.5 440.0 
Property, plant, and equipment, at cost3,214.3 2,945.4 
Accumulated depreciation(1,084.5)(1,044.6)
Property, plant, and equipment, net$2,129.8 $1,900.8 

Depreciation expense was $48.0 million and $94.1 million for the three and six months ended December 31, 2020, respectively, and $40.1 million and $79.2 million, for the three and six months ended December 31, 2019, respectively. Depreciation expense includes amortization of assets related to finance leases. The Company charges repairs and maintenance costs to expense as incurred. The Company capitalized interest cost of $4.0 million and $10.2 million for the three and six months ended December 31, 2020, respectively.
Other accrued liabilities
Other accrued liabilities consist of the following:
(Dollars in millions)December 31,
2020
June 30,
2020
Accrued employee-related expenses$151.9 $140.8 
Restructuring accrual6.5 2.8 
Accrued interest30.0 29.1 
Contract liability260.6 191.0 
Accrued income tax0.2 4.5 
Current liabilities held for sale (1)
19.9��
Other accrued liabilities and expenses126.0 131.1 
Total other accrued liabilities$595.1 $499.3 
(1) Represents current liabilities associated with the Company's Blow-Fill-Seal Business. See Note 3, Business Combinations and Divestitures for more details.
(Dollars in millions)December 31,
2021
June 30,
2021
Accrued employee-related expenses$136 $184 
Operating lease liabilities14 16 
Restructuring accrual
Accrued interest33 27 
Contract liabilities271 305 
Accrued income tax20 30 
Other178 170 
Total other accrued liabilities$653 $736 

17.     SUBSEQUENT EVENTS
Acorda Therapeutics, Inc. Purchase Agreement

In January 2021, the Company entered into an agreement to acquire the manufacturing and packaging operations of Acorda Therapeutics, Inc.'s (“Acorda”) dry powder inhaler and spray dry manufacturing business for $80.0 million, subject to customary adjustments. In connection with the sale, Acorda and the Company have entered into a long-term supply agreement under which the Company will manufacture and package INBRIJA® for Acorda. Upon closing, the facility and operations will become part of the Company’s Oral and Specialty Delivery segment. The agreement is subject to customary closing conditions and is expected to close during the third quarter of fiscal 2021.

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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 technologies,provide differentiated development and manufacturing solutions for drugs, protein-based biologics, cell and gene therapies, and consumer health products at over fifty facilities across four continents under rigorous quality and operational standards. Our oral, injectable, and respiratory delivery technologies, along with our state-of-the-art protein nucleic acid,and cell and gene therapy biologics,manufacturing capacity, address a wide and growing range of modalities and therapeutic and other categories across the biopharmaceutical and consumer health products. Our oral, injectable, cell and gene therapy, and respiratory delivery technologies address the full diversity of the pharmaceutical industry, including small molecules; protein, cell, and gene therapy biologics; and consumer health products.industries. Through our extensive capabilities, growth-enabling capacity, and deep expertise in product development, regulatory compliance, and clinical trial supply, we can help our customers take products to market faster, including nearly half of new drug products approved by the U.S. Food and Drug Administration (the “FDA”) in
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the last decade. Our advanced delivery technologydevelopment and manufacturing platforms, which include those in our Biologics, Softgel and Oral Technologies, Biologics, and Oral and Specialty Delivery segments, our proven formulation, manufacturing,supply, and regulatory expertise, and our broad and deep intellectual propertydevelopment and manufacturing know-how enable our customers to developadvance and then bring to market more products and better treatments for patients and consumers. Across both development and delivery, ourOur commitment to reliably supply our customers’ and their patients'patients’ needs is the foundation for the value we provide; annually, we produce approximately 74more than 70 billion doses for nearly 7,000 customer products, or approximately 1 in every 2024 doses of such productproducts 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 and 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 marginsattract premium opportunities and realize the growth potential from these areas.
We currently operate in four operating segments, which also constitute our four reporting segments: Biologics, Softgel and Oral Technologies, Oral and Specialty Delivery, and Clinical Supply Services.
The COVID-19 Pandemic
Our response to COVID-19
The
Since the start of the COVID-19 pandemic, has spread across the globe and is affecting economic activity worldwide, including in the countries in which we our customers, our suppliers, and our other business partners conduct business. Governments in affected regions have implemented, and may continue to implement, measures to protect public health, including quarantines, travel restrictions, business closures, cancellations of public gatherings, and measures that affect the flow of goods, services, and people between different regions. We have taken and continue to take steps to avoid or reduce infection or contamination and otherwise protect our employees, ensure the integrity and quality of our products and services, and to maintain business in line with guidelines issued bycontinuity for our customers and their patients who depend on us to manufacture and supply critical products to the U.S. Centers for Disease Control and Prevention (CDC), the World Health Organization (WHO), and local authorities where we operate, to re-emphasize good hygiene practices, severely restrict non-employee access to our sites, reorganize our workflows where permitted to maximize social distancing, limit our employees to only business-critical travel (where permitted by local law), facilitate safer alternatives to travel to and from work, and employ remote-working strategies. In addition, tomarket. To address the multiple dimensions of the pandemic, senior, multi-disciplinary teams reporting directly to our Chief Executive Officer have been continuously monitoring the global situation, executing mitigation activities whenever and wherever required, and planning forimplementing a phased and structured return to our facilities as circumstances will permithave permitted for those employees who have been remote-working.working remotely.

Among other things, we implemented measures to avoid or reduce infection or contamination in line with guidelines issued by the U.S. Centers for Disease Control and Prevention, the World Health Organization, and local authorities where we operate, re-emphasized good hygiene practices, restricted non-employee access to our sites, reorganized our workflows where permitted to maximize physical distancing, limited employee travel, facilitated safer alternatives to travel to and from work, and employed remote-working strategies. We have reviewed and will continue to analyze our supply chain to identify any risk, delay, or concern that may have an impact on our ability to deliver our services and products. To date, we have not identified any significant risk, delay, or concern that would have a substantial effect on such delivery. We have adopted various procedures to minimize and manage any future disruption to our ongoing operations. These include procuring expanded safety stocksoperations, including the creation and activation of raw materialsnew and personal protective equipment across our network, as well as ongoing monitoring of our suppliers’ stock levels to assure future deliveries.existing business continuity plans when needed. Our existing procedures, which are consistent with cGMPcurrent good manufacturing practices and other regulatory standards, are intended to assure the integrity of our supply including against any contamination. We have a detailed response plan to manage any impact of the virus on employee health, site operations, and product supply, including immediate assessment of the health of employees reporting symptoms, comprehensive risk assessment of any impact to quality, additional cleaning protocols, and alternative shift patterns to compensate should fewer employees be available.
The
Impact of COVID-19 pandemic has not had a material adverseon Our Business and Results of Operations

We continue to assess any impact on our business, financial condition, or results of operations to date, but, at this point, the extent to which the COVID-19 pandemic may affect our future financial condition or results of operations remains uncertain and will depend on future developments that are highly uncertain, including the duration of the pandemic, new information that may emerge concerning the severity of the virus, and the actions governments, the pharmaceutical industry, competitors, suppliers, customers, patients, and others may take to contain or address its direct and indirect effects. The COVID-19 pandemic and associated mitigation measures may also have an adverse impact on healthcare systems, global economic conditions, or economic conditions in one or more regions where we, our suppliers, or our customers operate, which could have an adverse effect on our business and financial condition.results of operations. We have observed some increases in customer delays and cancellations, occasional increases in absenteeism of production employees in our facilities in certain affected regions, and a small percentage of our customers expecting a reduction inseen increased demand and a larger percentage expecting an increase in demand, in each case due to circumstances relating to the COVID-19 pandemic and the responsive measures. We have also seensignificant revenue increases and the potential for further revenue increases from COVID-19-related products, particularly in our Biologics segment. As part of our response to the COVID-19 pandemic, we accelerated and enhanced certain of our capital improvement plans to expand capacity for manufacturing drug substance and drug product for protein-based biologics and cell and gene therapies, particularly at our drug product facilities in Bloomington, Indiana, and Anagni, Italy, as well as our commercial-scale viral vector manufacturing facility in Maryland. We have also implemented various strategies to protect our financial condition and results of operations should we experience a reduction in demand for COVID-19 related products, such as ensuring contractual take-or-pay and minimum volume requirements for the manufacture of certain COVID-19 related products. However, the extent and duration of revenue associated with COVID-19-related products is uncertain and dependent, in important respects, on factors outside our control.

The COVID-19-vaccines we manufacture are still pending approval from the FDA and other non-U.S. regulatory authorities and may not receive approval. The future duration and extent of the COVID-19 pandemic and the future demand for COVID-19 vaccines and therapies is unknown. Public opinion of certain COVID-19 vaccines and therapies and the product owners and manufacturers can change quickly and affect the demand for certain products and services, although they should not affect any required minimum payment for a COVID-19 related product subject to projects seeking to address thea “take-or-pay” provision. In addition, any
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concentration of revenue from certain COVID-19 pandemic or its effects. Future financial periods may reflect greater effectsvaccine products enhances our operational risk with respect to quality, security, regulatory inspections and business disruption resulting from any unforeseen event that affects any of the pandemic on the resultsfacilities and communities in which we manufacture COVID-19 vaccines. Because some of our operations.
See also “Risk Factors — Risks Relatedwork on COVID-19 vaccines is performed under subcontracts to Our BusinessU.S. government contracts, new regulations affecting U.S. federal government prime and Industry — Oursubcontractors may affect our operations, efficiency, and ability to deliver on our obligations to customers for COVID-19 vaccines, other COVID-19 related products, and other unrelated products and services. We have implemented various mechanisms to protect our customers, their material and product, and our business financial condition,continuity, such as enhanced security measures at certain facilities and results of operations may be adversely affected by global health epidemics, including the COVID-19 pandemic” in our Fiscal 2020 10-K.heightened cybersecurity controls.

Critical Accounting Policies and Estimates
We prepare our financial statements in accordance with generally accepted accounting principles in the United States (“U.S. GAAP”). Management made certain estimates and assumptions during the preparation of the consolidated financial statements in accordance with U.S. GAAP. These estimates and assumptions affect the reported amount of assets and liabilities and disclosures of contingent assets and liabilities in the consolidated financial statements. 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 estimates have a more significant impact on the consolidated financial statements than others.
There was no material change to our critical accounting policies or in the underlying accounting assumptions and estimates from those described in our Fiscal 20202021 10-K, other than recently adopted accounting principles disclosed in Note 1,Basis of Presentation and Summary of Significant Accounting Policies to the unaudited consolidated financial statements included elsewhere in this Quarterly Report on Form 10-Q (the “Consolidated Financial Statements”), which adoptions had no material impact on net earnings.our financial condition or results of operations.
Non-GAAP Metrics
EBITDA from operations
Management measures operating performance based on consolidated earnings from operations before interest expense, expense (benefit) for income taxes, and depreciation and amortization, adjusted for the income or loss attributable to non-controlling interests (EBITDA from operations”). EBITDA from operations is not defined under U.S. GAAP, is not a measure of 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 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 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 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 operations in order to provide supplemental information that we consider relevant for the readers of our Consolidated Financial Statements, and such information is not meant to replace or supersede U.S. GAAP measures. Our definition of EBITDA from operations may not be the same as similarly titled measures used by other companies. The most directly comparable measure to EBITDA from operations defined under U.S. GAAP is net earnings. Included in this Management’s Discussion and Analysis is a reconciliation of net earnings to EBITDA from operations.
In addition, we evaluate the performance of our segments based on segment earnings before non-controlling interests, other expense (income) expense,, impairments, restructuring costs, interest expense, income tax expense (benefit), and depreciation and amortization (Segment EBITDA”).
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-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-currency information compares results between periods as if exchange rates had remained constant period-over-period. We use results on a constant-currency basis as one measure to evaluate our performance. In this Quarterly Report on Form 10-Q, we compute constant currency by calculating current-year results using prior-year foreign currency exchange rates. We generally refer to such amounts calculated on a
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constant-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-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.
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Other Non-GAAP Measures
Organic revenue growth and Segment EBITDA growth are measures we use to explain the underlying results and trends in the business. Organic revenue growth and Segment EBITDA growth are measures used to show current year sales and earnings from existing operations and include revenue from licensing related activities entered into within the year.operations. Organic revenue growth and Segment EBITDA growth exclude the impact of foreign currency exchange, acquisitions of operating or legal entities, and divestitures within the year. 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, 20202021 Compared to the Three Months Ended December 31, 20192020
The below tables summarize several financial metrics we use to measure performance for the three months ended December 31, 20202021 and three months ended December 31, 2019.2020. Refer to the discussions below regarding performance and use of key financial metrics.
ctlt-20201231_g1.jpgctlt-20211231_g2.jpgctlt-20201231_g2.jpgctlt-20211231_g3.jpg
Results for the three months ended December 31, 20202021 compared to the three months ended December 31, 20192020 were as follows:        
Three Months Ended  
December 31,
FX ImpactConstant Currency Increase/(Decrease) Three Months Ended  
December 31,
FX ImpactConstant Currency Increase (Decrease)
(Dollars in millions)(Dollars in millions)20202019Change $Change %(Dollars in millions)20212020Change $Change %
Net revenueNet revenue$910.8 $721.4 $17.9 $171.5 24 %Net revenue$1,217 $911 $(13)$319 35 %
Cost of salesCost of sales612.6 489.2 10.9 112.5 23 %Cost of sales812 613 (8)207 34 %
Gross marginGross margin298.2 232.2 7.0 59.0 25 %Gross margin405 298 (5)112 38 %
Selling, general, and administrative expensesSelling, general, and administrative expenses165.5 141.0 1.4 23.1 16 %Selling, general, and administrative expenses228 165 (1)64 38 %
Impairment charges and (gain) loss on sale of assets0.6 1.7 — (1.1)(65)%
Restructuring and other5.5 0.5 0.1 4.9 980 %
Other operating expenseOther operating expense16 (1)11 185 %
Operating earningsOperating earnings126.6 89.0 5.5 32.1 36 %Operating earnings161 127 (3)37 30 %
Interest expense, netInterest expense, net25.9 34.9 0.2 (9.2)(26)%Interest expense, net32 26 — 24 %
Other (income) expense, net(8.3)(4.4)1.8 (5.7)130 %
Other expense (income), netOther expense (income), net14 (8)(2)24 (292)%
Earnings before income taxesEarnings before income taxes109.0 58.5 3.5 47.0 80 %Earnings before income taxes115 109 (1)%
Income tax expenseIncome tax expense20.6 13.0 0.7 6.9 53 %Income tax expense18 21 — (3)(14)%
Net earnings$88.4 $45.5 $2.8 $40.1 88 %
Net earningsNet earnings$97 $88 $(1)$10 11 %

Change % calculations are based on amounts prior to rounding

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Net Revenue
20202021 vs. 20192020
 Factors Contributing to Year-Over-Year ChangeThree Months Ended  
December 31,
Net Revenue
Net revenue without acquisitionsOrganic1732 %
Impact of acquisitions76 %
Constant currencyImpact of divestitures(3)%
Constant-currency change2435 %
Foreign currency translation impact on reporting(1)%
Total % change2634 %

Net revenue increased $171.5$319 million, or 24%35%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2019.2020. Net revenue decreased 3% inorganically principally due to the sale of Catalent USA Woodstock, Inc. and certain related assets (collectively, the “Blow-Fill-Seal Business”) in March 2021. Net revenue increased 7% as a result of acquisitions. We acquired a facility in Anagni, Italy (“Anagni”) in January 2020, Masthercell Global Inc. (“MaSTherCell”) in February 2020, and Skeletal Cell Therapy Support SA ("Skeletal") in November 2020. Net revenue increased 17% without the impact of acquisitions32% organically on a constant-currency basis, primarily due to robust(i) broad-based strength across our Biologics segment in part related to demand across all Biologics offerings, in particular demand for our drug product and drug substance offerings for COVID-19-related programs, offset in part due to decreasedand (ii) increased demand for our customers' prescription andproducts, a continued rebound in our consumer health products, particularly in thecough, cold, and over-the-counter pain relief products, and growth in development services in our Softgel and Oral Technologies segment. For the three months ended December 31, 2020, the favorable impact COVID-19-related programs had on Biologics net revenue was partially offset by an unfavorable impact due to demand decreases attributable to the COVID-19 pandemic on Softgel and Oral Technologies' net revenue.
Gross Margin
Gross margin increased $59.0$112 million, or 25%38%, compared to the three months ended December 31, 2019,2020, excluding the impact of foreign exchange, primarily as a result of the strong margin profile for allon broad-based offerings in our Biologics segment, offerings, including demand across our drug product and drug substance offeringsin part for COVID-19 related programs, offset by decreaseda favorable impact from the decline in recall charges in our Oral and Specialty Delivery segment, and increased demand for our prescription products and consumer health productsdevelopment growth in theour Softgel and Oral Technologies segment.segment, partially offset by a $13 million increase in depreciation and amortization expense. On a constant-currency basis, gross margin, as a percentage of revenue, increased 4060 basis points to 32.6%33.3% in the three months ended December 31, 2020,2021, compared to 32.2%32.7% in the prior-year period, primarily due to the factors described above.
Selling, General, and Administrative Expenses

Selling, general, and administrative expenses increased by $23.1$64 million, or 16%38%, compared to the three months ended December 31, 2019,2020, excluding the impact of foreign exchange, due towhich includes $15 million in net incremental expenses from acquired companies of $5.6 million, which includes $1.1 million of incremental depreciation and amortization expense, $2.0 million of employee-related costs and $1.9 million related to various transitional services.divested companies. The year-over-year increase in selling, general, and administrative expenses was alsoprimarily due to a $13.7an $18 million increase in employee-related costs primarilyprincipally incurred for wages and bonuses, which was partially offset by $6.4$13 million in transaction and integration costs savingsprimarily associated with healthour acquisition of Bettera Holdings, LLC (“Bettera”), $5 million of amortization and welfaredepreciation, and $3.3$4 million in cost savings associated with travel and entertainment.of bad debt expense.

Other Operating Expense
Additionally, selling, general, and administrative expenses were further increased by $9.8 million related to increases in information technology expenses associated with headcount increases and additional cyber security initiatives, insurance premium increases, certain market research initiatives, and COVID-19-related spend for personal protective equipment and test kits for our employees.
Restructuring and Other
Restructuring and other charges of $5.5 million operating expense for the three months ended December 31, 20202021 increased by $5.0 million, compared to the three months ended December 31, 2019. Restructuring expense varies period-to-period based on site consolidation efforts and other efforts to further streamline the business. In the three months ended December 31, 2020, we adopted a plan to reduce costs and optimize our Clinical Supply Services infrastructure in Western Europe by closing our facility in Bolton, U.K. and moving services to other locations in the region. In connection with this restructuring plan, we expect to reduce our headcount by approximately 150 to 180 employees through December 31, 2021 and incur charges between $4.0 million and $7.0 million primarily associated with employee severance benefits. For the three months ended December 31, 2020, we recognized $4.0 million of restructuring charges in association with the Bolton facility closure.
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Interest Expense, net
Interest expense, net of $25.9 million for the three months ended December 31, 2020 decreased by $9.2$11 million, or 26%185%, compared to the three months ended December 31, 2019,2020, when excluding the impact of foreign exchange, driven by savings from repaymentexchange. The year-over-year increase was primarily due to a $15 million increase in fixed asset impairment charges primarily associated with a product in our respiratory and specialty platform.
Interest Expense, net
Interest expense, net of Operating Company’s formerly outstanding euro-denominated term loan, euro-denominated 4.75% senior notes due 2024 and favorable interest rate movement on the U.S. dollar-denominated term loan, partially offset by interest expenses on Operating Company's euro-denominated 2.375% senior notes due 2028 (the “Euro 2028 Notes”). The savings also includes $4.0$32 million of capitalized interest costs for the three months ended December 31, 2020.2021 increased $6 million, or 24%, compared to the three months ended December 31, 2020, excluding the impact of foreign exchange. The savings from repayment of our formerly outstanding term loans and 4.875% senior notes due 2026 were offset by increases in interest expense due to our most recent tranche of term loans, 3.125% senior notes due 2029 (the “2029 Notes”), and 3.500% senior notes due 2030 (the “2030 Notes”).
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” and Note 6, Long-Term Obligations and Short-Term Borrowings to our Consolidated Financial Statements.
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Other (Income) Expense (Income), net
Other expense, net of $14 million for the three months ended December 31, 2021 was primarily driven by $15 million of foreign currency losses.

Other income, net of $8.3$8 million for the three months ended December 31, 2020 was primarily driven by a gain of $7.0$7 million related to the change in the fair value of the derivative liability arising from the dividend-adjustment mechanism of our seriesformerly outstanding Series A convertible preferred stock, par value $0.01 (the “Series A Preferred Stock”). See Notes 10 and 13 to our Consolidated Financial Statements for more details on the Series A Preferred Stock dividend-adjustment mechanism.

Other income, net of $4.4 million for the three months ended December 31, 2019 was primarily driven by a gain of $10.3 million related to the change in the fair value of the derivative liability arising from the dividend-adjustment mechanism of the Series A Preferred Stock. The gain was partially offset by non-cash foreign currency translation losses of $5.5 million.
Income Tax Expense
Our provision for income taxes for the three months ended December 31, 20202021 was $20.6$18 million relative to earnings before income taxes of $109.0$115 million. Our provision for income taxes for the three months ended December, 31, 20192020 was $13.0$21 million relative to earnings before income taxes of $58.5$109 million. The increaseddecrease in income tax provision forwas primarily the current period was largely impacted by an increaseresult of a shift in pretax income across severalin international tax jurisdictions and partially offset by an increase in discrete benefit items including certain equity compensation deductions. Generally, fluctuations in our effectivewith favorable tax rate are due to changes in the geographic distribution of our pretax income 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.rates.
Segment Review
The following charts depict the percentages of net revenue from each of our four reporting segments for the three months ended December 31, 20202021 compared to the three months ended December 31, 2019.2020. 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.
ctlt-20211231_g4.jpg

ctlt-20201231_g3.jpg
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Our results on a segment basis for the three months ended December 31, 20202021 compared to the three months ended December 31, 20192020 were as follows:
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Three Months Ended  
December 31,
FX ImpactConstant Currency Increase/(Decrease) Three Months Ended  
December 31,
FX ImpactConstant Currency Increase (Decrease)
(Dollars in millions)(Dollars in millions)20202019Change $Change %(Dollars in millions)20212020Change $Change %
BiologicsBiologicsBiologics
Net revenueNet revenue$403.9 $225.2 $7.9 $170.8 76 %Net revenue$638 $404 $(6)$240 60 %
Segment EBITDASegment EBITDA$135.5 $63.0 $3.9 $68.6 109 %Segment EBITDA197 136 (2)63 47 %
Softgel and Oral TechnologiesSoftgel and Oral TechnologiesSoftgel and Oral Technologies
Net revenueNet revenue246.6 267.9 5.2 (26.5)(10)%Net revenue329 247 (6)88 36 %
Segment EBITDASegment EBITDA45.6 64.5 1.0 (19.9)(31)%Segment EBITDA78 46 (1)33 73 %
Oral and Specialty DeliveryOral and Specialty DeliveryOral and Specialty Delivery
Net revenueNet revenue169.9 143.2 2.7 24.0 17 %Net revenue156 170 — (14)(8)%
Segment EBITDASegment EBITDA44.2 33.1 0.9 10.2 31 %Segment EBITDA44 44 — — — %
Clinical Supply ServicesClinical Supply ServicesClinical Supply Services
Net revenueNet revenue93.5 87.9 2.0 3.6 %Net revenue99 93 (2)%
Segment EBITDASegment EBITDA25.3 24.0 0.9 0.4 %Segment EBITDA27 25 (1)%
Inter-segment revenue eliminationInter-segment revenue elimination(3.1)(2.8)0.1 (0.4)(14)%Inter-segment revenue elimination(5)(3)(3)(61)%
Unallocated Costs (1)
Unallocated Costs (1)
(44.7)(29.3)(2.1)(13.3)(45)%
Unallocated Costs (1)
(101)(45)(58)(130)%
Combined totalsCombined totalsCombined totals
Net revenueNet revenue$910.8 $721.4 $17.9 $171.5 24 %Net revenue$1,217 $911 $(13)$319 35 %
EBITDA from operationsEBITDA from operations$205.9 $155.3 $4.6 $46.0 30 %EBITDA from operations$245 $206 $(2)$41 20 %
Change % calculations are based on amounts prior to rounding
(1)    Unallocated costs include restructuring and special items, stock-based compensation, impairment charges, certain other corporate directed costs, and other costs that are not allocated to the segments as follows:
Three Months Ended  
December 31,
Three Months Ended  
December 31,
(Dollars in millions)(Dollars in millions)20202019(Dollars in millions)20212020
Impairment charges and gain (loss) on sale of assets(a)Impairment charges and gain (loss) on sale of assets(a)$(0.6)$(1.7)Impairment charges and gain (loss) on sale of assets(a)$(16)$(1)
Stock-based compensationStock-based compensation(11.4)(10.3)Stock-based compensation(11)(11)
Restructuring and other special items (a)(b)
Restructuring and other special items (a)(b)
(14.7)(7.9)
Restructuring and other special items (a)(b)
(23)(15)
Other income, net (b)
8.3 4.4 
Other (expense) income, net (c)
Other (expense) income, net (c)
(14)
Unallocated corporate costs, netUnallocated corporate costs, net(26.3)(13.8)Unallocated corporate costs, net(37)(26)
Total unallocated costsTotal unallocated costs$(44.7)$(29.3)Total unallocated costs$(101)$(45)
(a)    Impairment charges and gain (loss) on sale of assets during the three months ended December 31, 2021 include fixed asset impairment charges associated with a product in our respiratory and specialty platform.
(b)    Restructuring and other special items during the three months ended December 31, 20202021 include (i) transaction and integration costs primarily associated with our Anagni, MaSTherCell, and Skeletal acquisitions. Charges for the quarter also include transaction costs for the saleacquisition of our blow-fill-seal manufacturing business, including 100% of the shares of Catalent USA Woodstock, Inc. (the “Blow-Fill-Seal Business”) andBettera, (ii) restructuring costs associated with the closure of our Clinical Supply Services facility in Bolton, U.K. Restructuring and other special items during the three months ended December 31, 20192020 include transaction costs for the sale of our Blow-Fill-Seal Business, and integrationrestructuring costs associated with the closure of our cell and gene therapy acquisitions, the disposal of a facility in Australia, and other restructuring initiatives across our network of sites.Bolton facility.
(b)(c)    Refer to Note 8, Other (income) expense, netExpense (Income), Net for details of financing charges and foreign currency translation adjustments recorded within other income (expense)expense (income), net in our Consolidated Financial Statements.
Provided below is a reconciliation of net earnings to EBITDA from operations:
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Three Months Ended  
December 31,
Three Months Ended  
December 31,
(Dollars in millions)(Dollars in millions)20202019(Dollars in millions)20212020
Net earningsNet earnings$88.4 $45.5 Net earnings$97 $88 
Depreciation and amortizationDepreciation and amortization71.0 61.9 Depreciation and amortization98 71 
Interest expense, netInterest expense, net25.9 34.9 Interest expense, net32 26 
Income tax expense20.6 13.0 
Income tax expense (benefit)Income tax expense (benefit)18 21 
EBITDA from operationsEBITDA from operations$205.9 $155.3 EBITDA from operations$245 $206 

Biologics segment
2020 vs. 2019
Factors Contributing to Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Net revenue/Segment EBITDA without acquisitions65 %104 %
Impact of acquisitions11 %%
Constant currency change76 %109 %
Foreign exchange fluctuation%%
Total % change79 %115 %
2021 vs. 2020
Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic59 %48 %
Impact of acquisitions%(1)%
Constant-currency change60 %47 %
Foreign exchange translation impact on reporting(2)%(2)%
Total % change58 %45 %
Biologics net revenue increased by $170.8$240 million, or 76%60%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2019.2020. The increase was driven by robust end-market demand for our drug product, drug substance and gene therapy offerings, in part related to demand for COVID-19 related programs.
Biologics Segment EBITDA increased by $63 million, or 47%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2020. The increase was driven by robust end-market demand for our drug product, drug substance and gene therapy offerings, in part related to demand for COVID-19 related programs.     
Softgel and Oral Technologies segment
2021 vs. 2020
Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic14 %43 %
Impact of acquisitions22 %30 %
Constant-currency change36 %73 %
Foreign currency translation impact on reporting(3)%(3)%
Total % change33 %70 %

Softgel and Oral Technologies net revenue increased by $88 million, or 36%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2020. The increase in organic revenue was driven by strong end-market demand for prescription products, a continued rebound in consumer health products, particularly in cough, cold, and over-the-counter pain relief products, and growth in development services.
Softgel and Oral Technologies Segment EBITDA increased $33 million, or 73%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2020. The organic portion of the increase, similar to that of net revenue, was driven by an increase in end-market demand in prescription products, a continued rebound in consumer health products, particularly in cough, cold, and over-the-counter pain relief products, and growth in development services.
We completed the Bettera acquisition in October 2021, which increased net revenue and Segment EBITDA on an inorganic basis by 22% and 30%, respectively, in the three months ended December 31, 2021, compared to the corresponding prior-year period.
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Oral and Specialty Delivery segment
2021 vs. 2020
Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic%24 %
Impact of acquisitions%(7)%
Impact of divestitures(15)%(17)%
Constant currency change(8)% %
Foreign currency translation impact on reporting— %— %
Total % change(8)%— %

Oral and Specialty Delivery net revenue decreased by $14 million, or 8%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2020. Net revenue increased 65%5%, compared to the three months ended December 31, 2019,2020, excluding the impact of acquisitions and divestitures, primarily driven by demand for early-phase development programs and orally delivered Zydis commercial products.
Oral and Specialty Delivery Segment EBITDA remained unchanged, excluding the impact of foreign exchange, compared to the three months ended December 31, 2020. Segment EBITDA increased 24%, compared to the three months ended December 31, 2020, excluding the impact of acquisitions and divestitures. The increase in Segment EBITDA from the prior-year period was primarily driven by the increased demand for commercial products and a favorable impact from prior year recall costs in our respiratory and specialty platform.
We completed the acquisition of the manufacturing and packaging operations of the Acorda Therapeutics, Inc. (“Acorda”) dry powder inhaler and spray dry manufacturing business in February 2021. For the three months ended December 31, 2021, this acquisition increased our net revenue and unfavorably impacted Segment EBITDA on an inorganic basis by 2% and 7%, respectively, compared to the corresponding prior-year period.
We completed the Blow-Fill-Seal Business divestiture in March 2021. For the three months ended December 31, 2021, this divestiture decreased our net revenue and unfavorably impacted Segment EBITDA on an inorganic basis by 15% and 17%, respectively, compared to the corresponding prior-year period.
Clinical Supply Services segment
2021 vs. 2020
Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic%%
Constant currency change7 %9 %
Foreign currency translation impact on reporting— %(1)%
Total % change%%
Clinical Supply Services net revenue increased by $8 million, or 7%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2020. The increase was driven by growth in our manufacturing and packaging and storage and distribution offerings in North America.
Clinical Supply Services Segment EBITDA increased $3 million, or 9%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2020. The increase was driven by demand in our manufacturing and packaging and storage and distribution offerings in North America.
Six Months Ended December 31, 2021 Compared to the Six Months Ended December 31, 2020
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The below tables summarize several financial metrics we use to measure performance for the six months ended December 31, 2021 and six months ended December 31, 2020. Refer to the discussions below regarding performance and use of key financial metrics.

ctlt-20211231_g5.jpgctlt-20211231_g6.jpg
Results for the six months ended December 31, 2021 compared to the six months ended December 31, 2020 were as follows:
 Six Months Ended  
December 31,
FX ImpactConstant Currency Increase (Decrease)
(Dollars in millions)20212020Change $Change %
Net revenue$2,242 $1,757 $(6)$491 28 %
Cost of sales1,513 1,210 (4)307 25 %
Gross margin729 547 (2)184 34 %
Selling, general, and administrative expenses411 330 — 81 24 %
Gain on sale of subsidiary(1)— — (1)*
Other operating expense20 (1)12 138 %
Operating earnings299 208 (1)92 44 %
Interest expense, net58 51 12 %
Other expense (income), net23 (19)(1)43 (223)%
Earnings before income taxes218 176 (1)43 24 %
Income tax expense28 — 23 400 %
Net earnings$190 $171 $(1)$20 11 %
Change % calculations are based on amounts prior to rounding 
*Percentage not meaningful
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Net Revenue
2021 vs. 2020
Year-Over-Year ChangeSix Months Ended  
December 31,
Net Revenue
Organic27 %
Impact of acquisitions%
Impact of divestitures(3)%
Constant currency change28%
Foreign currency translation impact on reporting— %
Total % change28 %
Net revenue increased by $491 million, or 28%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2020. Net revenue increased 4% inorganically as a result of acquisitions, which was partially offset by a 3% decrease in net revenue due to the sale of our Blow-Fill-Seal Business. We acquired Skeletal Cell Therapy Support (“Skeletal”) in November 2020, Delphi Genetics SA (“Delphi”) and the manufacturing and packaging assets of Acorda in February 2021, and Bettera in October 2021. Net revenue increased 27% organically on a constant-currency basis, primarily related to (i) robust demand across all our Biologics offerings, in particular demand for our drug product and drug substance offerings for COVID-19-related programs, (ii) increased demand for our customers' prescription products, a continued rebound in our consumer health products, particularly in cough, cold, and over-the-counter pain relief products, and growth in development services in our Softgel and Oral Technologies segment.
Gross Margin
Gross margin increased by $184 million, or 34%, compared to the six months ended December 31, 2020, excluding the impact of foreign exchange, primarily due to the strong margin profile for all Biologics segment offerings, including demand across our drug product and drug substance offerings for COVID-19 related programs. Additional factors for such growth included an increased demand for prescription products and continued rebound in consumer health products in our Softgel and Oral Technologies segment and a favorable impact from the decline in recall charges in our Oral and Specialty Delivery segment. Margin growth was offset in part by a $23 million increase in depreciation and amortization expense. On a constant-currency basis, gross margin, as a percentage of revenue, increased 140 basis points to 32.5% in the six months ended December 31, 2021, compared to 31.1% in the corresponding prior-year period.
Selling, General, and Administrative Expenses

Selling, general, and administrative expenses increased by $81 million, or 24%, compared to the six months ended December 31, 2020, excluding the impact of foreign exchange, which includes $16 million in net incremental expenses from acquired and divested companies. The year-over-year increase in selling, general and administrative expenses was primarily due to $28 million for employee-related costs principally incurred for wages and bonuses, $16 million in transaction and integration costs primarily associated with our Bettera acquisition, $6 million of incremental depreciation and amortization expense, a $6 million increase in information technology spend associated with additional cyber security initiatives, and $4 million of bad debt expense, partially offset by $4 million in cost savings associated with employee health and welfare costs.
Other Operating Expense
Other operating expense of $20 million for the six months ended December 31, 2021 increased by $12 million, or 138%, compared to the six months ended December 31, 2020, excluding the impact of foreign exchange. The year-over-year increase was primarily due to a $15 million increase in fixed asset impairment charges associated with a product in our respiratory and specialty platform.
Interest Expense, net
Interest expense, net of $58 million for the six months ended December 31, 2021 increased by $6 million, or 12%, compared to the six months ended December 31, 2020, excluding the impact of foreign exchange. The savings from repayment of our formerly outstanding term loans and 4.875% senior notes due 2026 were offset by increases in interest expense due to our most recent tranche of term loans, the 2029 Notes, and the 2030 Notes. The savings also includes a $3 million reduction in capitalized interest costs for the six months ended December 31, 2021.
Other Expense (Income), net
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Other expense, net of $23 million for the six months ended December 31, 2021 was primarily driven by $24 million of foreign currency losses, $4 million of financing charges related to our outstanding term loans, partially offset by a $2 million gain related to the change in fair value of the derivative liability arising from the dividend-adjustment mechanism of our formerly outstanding Series A Preferred Stock.
Other income, net for the six months ended December 31, 2020 of $19 million was primarily driven by a gain of $16 million related to the change in fair value of the derivative liability arising from the dividend-adjustment mechanism of our Series A Preferred Stock.
Income Tax Expense
Our provision for income taxes for the six months ended December 31, 2021 was $28 million relative to earnings before income taxes of $218 million. Our provision for income taxes for the six months ended December 31, 2020 of $5 million relative to earnings before income taxes of $176 million. The increase in the provision was the result of a decrease in non-U.S. tax credits claimed on an amended U.S. federal income tax filing compared to the prior-year period. The provision for income taxes in each of these periods was also impacted by the relative amount and mix of permanent tax adjustments included in the income tax computation and other discrete tax items recognized in the periods.
Segment Review
The below charts depict the percentage of revenue for each of our four segments for the six months ended December 31, 2021 compared to the six months ended December 31, 2020. Refer below for discussions regarding each segment's revenue and EBITDA performance.
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Our results on a segment basis for the six months ended December 31, 2021 compared to the six months ended December 31, 2020 were as follows:
 Six Months Ended  
December 31,
FX ImpactConstant Currency Increase/(Decrease)
(Dollars in millions)20212020Change $Change %
Biologics
Net revenue$1,184 $781 $(5)$408 52 %
Segment EBITDA363 242 (1)122 50 %
Softgel and Oral Technologies
Net revenue572 468(4)108 23 %
Segment EBITDA119 83(1)37 44 %
Oral and Specialty Delivery
Net revenue302 328 (30)(9)%
Segment EBITDA77 66 15 %
Clinical Supply Services
Net revenue195 186 — %
Segment EBITDA53 50 — %
Inter-segment revenue elimination(11)(6)(1)(4)(67)%
Unallocated Costs (1)
(157)(74)— (83)(114)%
Combined totals
Net revenue$2,242 $1,757 $(6)$491 28 %
EBITDA from operations$455 $367 $— $88 24 %
Change % calculations are based on amounts prior to rounding
(1) Unallocated costs include restructuring and special items, stock-based compensation, gain on sale of subsidiary, 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)20212020
Impairment charges and gain (loss) on sale of assets (a)
$(19)$(2)
Equity compensation(32)(30)
Restructuring and other special items (b)
(31)(20)
Gain on sale of subsidiary (c)
— 
       Other expense (income), net (d)
(23)19 
Non-allocated corporate costs, net(53)(41)
Total unallocated costs$(157)$(74)
(a) Impairment charges and gain (loss) on sale of assets during the six months ended December 31, 2021 include fixed asset impairment charges associated with a product in our respiratory and specialty platform.
(b) Restructuring and other special items during the six months ended December 31, 2021 include (i) transaction and integration costs associated with the acquisitions of Delphi, Hepatic Cell Therapy Support SA, RheinCell Therapeutics GmbH, and Bettera and, (ii) restructuring costs associated with the closure of the Bolton facility. Restructuring and other special items during the six months ended December 31, 2020 include transaction costs for the sale of our Blow-Fill-Seal Business, acquisitions of facilities in Italy and Belgium, disposal of a site in Australia, restructuring costs associated with the closure of the Bolton facility and other restructuring initiatives across our network of sites.
(c) For the six months ended December 31, 2021, gain on sale of subsidiary was due to the divestiture of our Blow-Fill-Seal Business.
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(d) Refer to Note 8, Other expense (income), net for details of financing charges and foreign currency translation adjustments recorded within other expense, net in our Consolidated Financial Statements.
Provided below is a reconciliation of net earnings to EBITDA from operations:
 Six Months Ended  
December 31,
(Dollars in millions)20212020
Net earnings$190 $171 
Depreciation and amortization179 140 
Interest expense, net58 51 
Income tax expense28 
EBITDA from operations$455 $367 
Biologics segment
2021 vs. 2020
Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic52 %51 %
Impact of acquisitions— %(1)%
Constant-currency change52 %50 %
Foreign exchange translation impact on reporting— %— %
Total % change52 %50 %
Net revenue in our Biologics segment increased by $408 million, or 52%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2020. The increase was driven across all segment offerings with robust end-market demand for our drug product, drug substance, and cell and gene therapy offerings, primarily related to demand for COVID-19-related programs.
Biologics Segment EBITDA increased by $122 million, or 50%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2020. Segment EBITDA increased 51%, compared to the six months ended December 31, 2020, excluding the impact of acquisitions. The increase was driven across all segment offerings with robust end-market demand for our global drug product, and drug substance, and cell and gene therapy offerings, primarily related to demand for COVID-19 relatedCOVID-19-related programs.
Biologics Segment EBITDASoftgel and Oral Technologies segment
2021 vs. 2020
Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic12 %28 %
Impact of acquisitions11 %16 %
Constant-currency change23 %44 %
Foreign exchange translation impact on reporting(1)%(2)%
Total % change22 %42 %

Softgel and Oral Technologies net revenue increased by $68.6$108 million, or 109%23%, excluding the impact of foreign exchange, compared to the threesix months ended December 31, 2019. Segment EBITDA2020. Net revenue increased 104%12%, compared to the threesix months ended December 31, 2019,2020, excluding the impact of acquisitions. The increase was driven across all segment offerings with robust end-market demand for our global drug product and drug substance offerings, predominantly related to demand for COVID-19 related programs.
Since December 30, 2019, we have acquired Anagni, part of which operates within the Biologics segment, MaSTherCell and Skeletal, which together increased netin organic revenue and Segment EBITDA on an inorganic basis in our Biologics segment by 11% and 5%, respectively, in the three months ended December 31, 2020 compared to the corresponding prior-year period.
Softgel and Oral Technologies segment
2020 vs. 2019
Factors Contributing to Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Net revenue/Segment EBITDA(10)%(31)%
Impact of acquisitions and divestitures— %— %
Constant currency change(10)%(31)%
Foreign currency translation impact on reporting%%
Total % change(8)%(29)%

Softgel and Oral Technologies net revenue decreased by $26.5 million, or 10%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2019. The decrease primarily relates to reduced end marketstrong end-market demand for prescription products, within North America and Europe, as well as lower demanda continued rebound in consumer health products, particularly in cough, cold, and over-the-counter pain relief products, attributable to effects of the COVID-19 pandemic. The net revenue decrease is partially offset by strongand growth in development revenue growth.services within North America
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Softgel and Oral Technologies Segment EBITDA decreased $19.9increased $37 million, or 31%44%, excluding the impact of foreign exchange, compared to the threesix months ended December 31, 2019.2020. Segment EBITDA increased 28% compared to the six months ended December 31, 2020, excluding the impact of acquisitions. The decrease,organic portion of the increase, similar to that of net revenue, iswas primarily driven by a decreasean increase in demand in both the prescription and consumer health portfolio of products, offset in part byas well as the margin generated from strong development revenue growth.
We completed the Bettera acquisition in October 2021, which increased net revenue and Segment EBITDA on an inorganic basis by 11% and 16%, respectively, in the six months ended December 31, 2021, compared to the corresponding prior-year period.
Oral and Specialty Delivery segment
2020 vs. 2019
Factors Contributing to Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Net revenue/Segment EBITDA without acquisitions%%
Impact of acquisitions15 %22 %
Constant currency change17 %31 %
Foreign currency translation impact on reporting%%
Total % change19 %34 %
2021 vs. 2020
Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic%50 %
Impact of acquisitions%(12)%
Impact of divestitures(14)%(23)%
Constant-currency change(9)%15 %
Foreign exchange translation impact on reporting%%
Total % change(8)%18 %
Net revenue in our Oral and Specialty Delivery net revenue increasedsegment decreased by $24$30 million, or 17%9%, compared to the six months ended December 31, 2020, excluding the impact of foreign exchange, compared to the three months ended December 31, 2019.exchange. Net revenue increased 2%4%, compared to the threesix months ended December 31, 2019,31. 2020, excluding the impact of acquisitions. Increasedacquisitions and divestitures, primarily driven by demand for the segment’s orally delivered Zydis commercial products and early-phase development programs were partially offset by decreased demand for other non-Zydis orally delivered commercial products.programs.
Oral and Specialty DeliveryDelivery’s Segment EBITDA increased by $10.2$9 million, or 31%15%, compared to the six months ended December 31, 2020, excluding the impact of foreign exchange,exchange. Segment EBITDA increased 50% compared to the threesix months ended December 31, 2019.2020, excluding the impact of acquisitions and divestitures. The organic portion of the increase from the corresponding prior-year period was primarily driven by increased demand for the segment’s orally delivered Zydis commercial products early-phase development programs and a favorable manufacturing efficiencies withinimpact from prior year recall costs in our respiratory and ophthalmicspecialty platform.
We acquired Anagni on January 1, 2020 and the portion of this facility allocated to our Oral and Specialty DeliveryClinical Supply Services segment increased
2021 vs. 2020
Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Organic%%
Constant-currency change5 %5 %
Foreign exchange translation impact on reporting— %%
Total % change%%
Clinical Supply Services’ net revenue and Segment EBITDA on an inorganic basisincreased by 15% and 22%$9 million, or 5%, respectively, incompared to the threesix months ended December 31, 2020, compared to the corresponding prior-year period.
Clinical Supply Services segment
2020 vs. 2019
Factors Contributing to Year-Over-Year ChangeThree Months Ended  
December 31,
Net RevenueSegment EBITDA
Net revenue/Segment EBITDA%%
Impact of acquisitions and divestitures— %— %
Constant currency change4 %2 %
Foreign currency translation impact on reporting%%
Total % change%%
Clinical Supply Services net revenue increased by $3.6 million, or 4%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2019.exchange. The increase was driven by strong demand in our manufacturing and packaging and storage and distribution offerings in North America.
Clinical Supply ServicesServices’ Segment EBITDA increased by $0.4$3 million, or 2%, excluding the impact of foreign exchange, compared to the three months ended December 31, 2019. The increase was driven by strong demand in our manufacturing and packaging and storage and distribution offerings in North America, partially offset by an unfavorable sales mix in Europe.
Six Months Ended December 31, 2020 Compared to the Six Months Ended December 31, 2019
The below tables summarize several financial metrics we use to measure performance for the six months ended December 31, 2020 and six months ended December 31, 2019. Refer to the discussions below regarding performance and use of key financial metrics.

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ctlt-20201231_g4.jpgctlt-20201231_g5.jpg
Results for the six months ended December 31, 2020 compared to the six months ended December 31, 2019 were as follows:        
 Six Months Ended  
December 31,
FX ImpactConstant Currency Increase/(Decrease)
(Dollars in millions)20202019Change $Change %
Net revenue$1,756.5 $1,386.1 $27.6 $342.8 25 %
Cost of sales1,209.4 976.2 16.7 216.5 22 %
Gross margin547.1 409.9 10.9 126.3 31 %
Selling, general, and administrative expenses330.2 283.8 2.4 44.0 16 %
Impairment charges and (gain) loss on sale of assets2.4 1.5 — 0.9 60 %
Restructuring and other6.4 1.2 0.1 5.1 425 %
Operating earnings208.1 123.4 8.4 76.3 62 %
Interest expense, net51.2 71.2 0.4 (20.4)(29)%
Other (income) expense, net(19.5)0.5 3.3 (23.3)*
Earnings before income taxes176.4 51.7 4.7 120.0 232 %
Income tax expense5.6 6.1 0.6 (1.1)(18)%
Net earnings$170.8 $45.6 $4.1 $121.1 266 %
*Percentage not meaningful
Net Revenue
2020 vs. 2019
 Factors Contributing to Year-Over-Year ChangeSix Months Ended  
December 31,
Net Revenue
Net revenue without acquisitions/divestitures19 %
Impact of acquisitions%
Impact of divestitures(1)%
Constant currency change25%
Foreign currency translation impact on reporting%
Total % change27 %
Net revenue increased by $342.8 million, or 25%5%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2019. Net revenue increased 7% as a result of acquisitions, which was partially offset by a 1% decrease in net revenue due to a facility divestiture. We acquired Anagni in January 2020, MaSTherCell in February 2020, and Skeletal in November 2020 and divested a facility in Australia in October 2019. Net revenue increased 19% without the impact of acquisitions and divestitures on a constant-currency basis, primarily related to robust demand across all our Biologics offerings,
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in particular demand for our drug product and drug substance offerings for COVID-19-related programs, offset in part due to decreased demand for our prescription and consumer health products in the Softgel and Oral Technologies segment. For the six months ended December 31, 2020, the favorable impact COVID-19-related programs had on Biologics net revenue was partially offset by an unfavorable impact due to demand decreases attributable to the COVID-19 pandemic on Softgel and Oral Technologies' net revenue.
Gross Margin
Gross margin increased by $126.3 million, or 31%, compared to the six months ended December 31, 2019, excluding the impact of foreign exchange, primarily as a result of the strong margin profile for all Biologics segment offerings, including demand across our drug product and drug substance offerings for COVID-19 related programs. Growth was offset in part by decreased demand for our prescription and consumer health products in the Softgel and Oral Technologies segment and a one-time charge totaling $14 million following the voluntary recall in the U.S. of a recently launched product in our respiratory and ophthalmic platform. On a constant-currency basis, gross margin, as a percentage of revenue, increased 140 basis points to 31% in the six months ended December 31, 2020, compared to 29.6% in the corresponding prior-year period, primarily due to recent acquisitions.
Selling, General, and Administrative Expenses

Selling, general, and administrative expenses increased by $44 million, or 16%, compared to the six months ended December 31, 2019, excluding the impact of foreign exchange, driven by additional selling, general and administrative expenses from acquired companies of $11.2 million, including $2.2 million of incremental depreciation and amortization expense, $3.8 million for employee-related costs and $3.6 million related to various transitional services. An additional $25.9 million of employee-related cost primarily incurred for wages and bonuses, was partially offset by $7.2 million in cost savings associated with health and welfare and $6.5 million in savings related to travel and entertainment expenses.

The year-over-year increase in selling, general, and administrative expenses was also due to a $17.2 million increase in information technology spend associated with headcount increases and additional cyber security initiatives, insurance premium increases, certain market research initiatives and COVID-19 related spend for personal protective equipment and test kits for our employees.
Restructuring and Other
Restructuring and other charges of $6.4 million for the six months ended December 31, 2020 increased by $5.2 million, compared to the six months ended December 31, 2019. Restructuring expense varies period-to-period based on site consolidation efforts and other efforts to further streamline the business. In the three months ended December 31, 2020, we adopted a plan to reduce costs and optimize our infrastructure in Western Europe by closing our Clinical Supply Services facility in Bolton, U.K. In connection with this restructuring plan, we expect to reduce our headcount by approximately 150 to 180 employees through December 31, 2021 and incur charges between $4.0 million to $7.0 million, primarily associated with employee severance benefits. For the six months ended December 31, 2020, we recognized $4.0 million of restructuring charges in association with the Bolton facility closure.
Interest Expense, net
Interest expense, net of $51.2 million for the six months ended December 31, 2020 decreased by $20.0 million, or 28%, compared to the six months ended December 31, 2019, driven by savings from repayment of Operating Company’s formerly outstanding euro-denominated term loan, euro-denominated 4.75% senior notes due 2024 and favorable interest rate movement on the U.S. dollar-denominated term loan, partially offset by interest expenses on Operating Company's Euro 2028 Notes. The savings also includes $10.2 million of capitalized interest costs for the six months ended December 31, 2020.
Other (Income) Expense, net
Other income, net of $19.5 million for the six months ended December 31, 2020 was primarily driven by a gain of $16.0 million related to the change in the fair value of the derivative liability arising from the dividend adjustment mechanism of the Series A Preferred Stock and a net foreign currency translation gain of $0.8 million.
Other expense, net for the six months ended December 31, 2019 of $0.5 million includes a gain of $1.4 million related to the change in the fair value of the derivative liability arising from the dividend adjustment mechanism of the Series A Preferred Stock, the foreign currency gain of $4.4 million and non-cash foreign currency translation losses of $8.0 million.
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Income Tax Expense
Our provision for income taxes for the six months ended December 31, 2020 was $5.6 million relative to earnings before income taxes of $176.4 million. Our provision for income taxes for the six months ended December 31, 2019 was $6.1 million relative to earnings before income taxes of $51.7 million. The reduced income tax provision for the current six-month period reflects an increase in the pretax earnings significantly offset by discrete items including a $22.2 million benefit for U.S. foreign tax credits resulting from amending a prior-year return. Generally, fluctuations in our effective tax rate are primarily due to changes in the geographic distribution of our pretax income 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.
Segment Review
The below charts depict the percentage of revenue for each of the Company's four segments for the six months ended December 31, 2020 compared to the six months ended December 31, 2019. Refer below for discussions regarding each segment's revenue and EBITDA performance.
ctlt-20201231_g6.jpg
Our results on a segment basis for the six months ended December 31, 2020 compared to the six months ended December 31, 2019 were as follows:

 Six Months Ended  
December 31,
FX ImpactConstant Currency Increase/(Decrease)
(Dollars in millions)20202019Change $Change %
Biologics
Net revenue$781.0 $413.8 $11.2 $356.0 86 %
Segment EBITDA242.0 98.8 5.0 138.2 140 %
Softgel and Oral Technologies
Net revenue467.7528.57.2$(68.0)(13)%
Segment EBITDA83.4110.91.8$(29.3)(26)%
Oral and Specialty Delivery
Net revenue328.2 275.8 5.6 46.8 17 %
Segment EBITDA65.6 60.8 2.0 2.8 %
Clinical Supply Services
Net revenue186.2 172.5 3.5 10.2 %
Segment EBITDA50.3 45.6 1.6 3.1 %
Inter-segment revenue elimination(6.6)(4.5)0.1 (2.2)(49)%
Unallocated Costs (1)
(73.6)(70.7)(3.8)0.9 %
Combined totals
Net revenue$1,756.5 $1,386.1 $27.6 $342.8 25 %
EBITDA from operations$367.7 $245.4 $6.6 $115.7 47 %
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(1) Unallocated costs include restructuring and special items, stock-based compensation, impairment charges, certain other corporate-directed costs, and other costs that are not allocated to the segments as follows:
 Six Months Ended  
December 31,
(Dollars in millions)20202019
Impairment charges and gain (loss) on sale of assets$(2.4)$(1.5)
Equity compensation(30.1)(26.9)
Restructuring and other special items (a)
(19.6)(19.7)
       Other income (expense), net (b)
19.5 (0.5)
Non-allocated corporate costs, net(41.0)(22.1)
Total unallocated costs$(73.6)$(70.7)
(a) Restructuring and other special items during the six months ended December 31, 2020 include transaction and integration costs associated with our Anagni, MaSTherCell, and Skeletal acquisitions. Charges for the period also include transaction costs for the sale of our Blow-Fill-Seal Business and restructuring costs associated with the closure of our Clinical Supply Services facility in Bolton, U.K. and the disposal of a facility in Australia. Restructuring and other special items during the six months ended December 31, 2019 include transaction and integration costs associated with our cell and gene therapy acquisitions, the disposal of a facility in Australia, and other restructuring initiatives across our network of sites.
(b) Refer to Note 8, Other (income) expense, net for details of financing charges and foreign currency translation adjustments recorded within other income (expense), net in our Consolidated Financial Statements.
Provided below is a reconciliation of net earnings to EBITDA from operations:
 Six Months Ended  
December 31,
(Dollars in millions)20202019
Net earnings$170.8 $45.6 
Depreciation and amortization140.1 122.5 
Interest expense, net51.2 71.2 
Income tax expense5.6 6.1 
EBITDA from operations$367.7 $245.4 
Biologics segment
2020 vs. 2019
Factors Contributing to Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Net revenue/Segment EBITDA without acquisitions73 %132 %
Impact of acquisitions13 %%
Constant currency change86 %140 %
Foreign exchange fluctuation%%
Total % change89 %145 %
Net revenue in our Biologics segment increased by $356.0 million, or 86%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2019. Net revenue increased 73%, compared to the six months ended December 31, 2019, excluding the impact of acquisitions. The increase was driven across all segment offerings with robust end-market demand for the global drug product, drug substance and cell and gene therapy, in part related to demand for COVID-19 related programs.
Biologics Segment EBITDA increased by $138.2 million, or 140%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2019. Segment EBITDA increased 132%, compared to the six months ended December 31, 2019, excluding the impact of acquisitions. The increase was driven across all segment offerings with robust end-market demand for the global drug product, drug substance, and cell and gene therapy offerings, in part related to demand for
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COVID-19-related programs. The increase in Segment EBITDA was partially offset by an increase in base costs associated with our commercial readiness activity across our cell and gene therapy offering.
Since December 30, 2019, we have acquired Anagni, part of which operates within the Biologics segment, MaSTherCell and Skeletal, which together increased net revenue and Segment EBITDA on an inorganic basis in our Biologics segment by 13% and 8%, respectively, in the six months ended December 31, 2020 compared to the corresponding prior-year period.
Softgel and Oral Technologies segment
2020 vs. 2019
 Factors Contributing to Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Net revenue/Segment EBITDA without divestitures(11)%(27)%
Impact of acquisitions and divestitures(2)%%
Constant currency change(13)%(26)%
Foreign exchange fluctuation%%
Total % change(12)%(25)%

Softgel and Oral Technologies’ net revenue decreased $68 million, or 13%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2019. Net revenue decreased 11%, compared to the six months ended December 31, 2019, excluding the impact of divestitures. The decrease primarily relates to reduced end market demand for prescription products within North America and Europe, as well as lower demand in consumer health products, particularly in cough, cold, and over-the-counter pain relief products attributable to the effects of the COVID-19 pandemic. The net revenue decrease is partially offset by strong development revenue growth.
Softgel and Oral Technologies’ Segment EBITDA decreased by $29.3 million, or 26%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2019. Segment EBITDA decreased 27%, compared to the six months ended December 31, 2019, excluding the impact of divestitures. The decrease, similar to that of net revenue, is primarily driven by a decrease in demand in both the prescription and consumer health portfolio of products, offset in part by the margin generated from strong development revenue growth.
In October 2019, we divested a manufacturing facility in Australia in order to better streamline our global operations. The facility divestiture resulted in a decrease in net revenue of 2% and an increase in Segment EBITDA of 1%, in the six months ended December 31, 2020 compared to the six months ended December 31, 2019.
Oral and Specialty Delivery segment
2020 vs. 2019
Factors Contributing to Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Net revenue/Segment EBITDA without acquisitions%(23)%
Impact of acquisitions16 %28 %
Constant currency change17 %5 %
Foreign exchange fluctuation%%
Total % change19 %%
Net revenue in our Oral and Specialty Delivery segment increased by $46.8 million, or 17%, compared to the six months ended December 31, 2019, excluding the impact of foreign exchange. Net revenue increased 1%, compared to the six months ended December 31, 2019, excluding the impact of acquisitions. Excluding the effect of acquisitions, increased demand for the segment’s orally delivered Zydis commercial products and early-phase development programs were partially offset by decreased demand for other non-Zydis orally delivered commercial products.
Oral and Specialty Delivery’s Segment EBITDA increased by $2.8 million, or 5%, compared to the six months ended December 31, 2019, excluding the impact of foreign exchange. Segment EBITDA decreased 23% compared to the six months ended December 31, 2019, excluding the impact of acquisitions. The decrease from the prior-year period was primarily driven by the voluntary recall in the U.S of a recently launched product in our respiratory and ophthalmic platform, inclusive of one-
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time charges totaling $14 million, associated with the recall. Increased demand for the segment’s orally delivered Zydis commercial products and favorable manufacturing efficiencies within our respiratory and ophthalmic specialty platform partially offset the charges associated with this product recall.
Clinical Supply Services segment
2020 vs. 2019
Factors Contributing to Year-Over-Year ChangeSix Months Ended  
December 31,
Net RevenueSegment EBITDA
Net revenue/Segment EBITDA%%
Impact of acquisitions and divestitures— %— %
Constant currency change6 %7 %
Foreign exchange fluctuation%%
Total % change%10 %
Clinical Supply Services’ net revenue increased by $10.2 million, or 6%, compared to the six months ended December 31, 2019, excluding the impact of foreign exchange. The increase was driven by strong demand in our manufacturing and packaging business across all regions and an increase in demand for our storage and distribution offerings in North America.
Clinical Supply Services’ Segment EBITDA increased by $3.1 million, or 7%, excluding the impact of foreign exchange, compared to the six months ended December 31, 2019, primarily due to strong global demand in our manufacturing and packaging and storage and distribution businesses, partially offset by an unfavorable sales mixoffering in Europe.North America.
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Liquidity and Capital Resources
Sources and Uses of Cash
Our principal sources of liquidity have been cash flows generated from operations and occasional capital market activities. The principal uses of cash are to fund operating and capital expenditures, business or asset acquisitions, interest payments on debt, the payment of deferred purchase consideration from the Catalent Indiana, LLC acquisition, the payment of the quarterly dividend on the Series A Preferred Stock, and any mandatory or discretionary principal payment on our debt. At the current stated value of the Series A Preferred Stock outstanding as of December 31, 2020, the aggregate amount of each regular quarterly dividend, if paid in cash, is $4.8 million. As of December 31, 2020,2021, Catalent Pharma Solutions, Inc., our principal operating subsidiary (“Operating Company”), following the Operating CompanySeptember 2021 execution of Amendment No. 6 to the amended and restated credit agreement, dated as of May 20, 2014, governing our senior secured credit facilities (as amended, the “Credit Agreement”), had available a $550$725 million revolving credit facility that matures in May 2024, the capacity of which was reduced by $6.7$5 million in letters of credit outstanding as of December 31, 2020.2021. The revolving credit facility includes borrowing capacity available for lettersletters of credit and for short-term borrowings, referred to as swing-line borrowings.
On October 1, 2021, we acquired Bettera, a manufacturer of nutraceuticals specializing in gummy, soft chew, and lozenge delivery systems paying approximately $1.00 billion in cash. We funded this acquisition through a combination of additional borrowings under our senior secured credit facilities and the net proceeds of the 2030 Notes.
We believe that our cash on hand, cash from operations, and available borrowings under our revolving credit facility will be adequate to meet our future liquidity needs for at least the next twelve12 months, including our quarterly regular dividend on the Series A Preferred Stock, if paid in cash, as well as the amounts expected to become due with respect to our pending capital projects. We have no significant maturity under any of our bank or note debt until the U.S. dollar-denominated 4.875%July 2027 maturity of our 5.000% senior notes due 20262027 (the “USD 2026"2027 Notes”) maturing in January 2026. As of December 31, 2020, we had only one remaining payment of $50.0 million, due in October 2021, on the deferred purchase consideration for the acquisition of Catalent Indiana, LLC..
Cash Flows
The following table summarizes our consolidated statements of cash flows:
 Six Months Ended  
December 31,
 
(Dollars in millions)20202019$ Change
Net cash provided by (used in):
Operating activities$223.7 $145.9 $77.8 
Investing activities$(354.4)$(199.2)$(155.2)
Financing activities$(7.2)$(101.8)$94.6 
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 Six Months Ended  
December 31,
 
(Dollars in millions)20212020$ Change
Net cash provided by (used in):
Operating activities$232 $224 $
Investing activities$(1,299)$(354)$(945)
Financing activities$1,033 $(7)$1,040 
Operating Activities
For the six months ended December 31, 2020,2021, cash provided by operating activities was $223.7$232 million, compared to $145.9$224 million for the corresponding prior-year period. CashThis increase in cash flow from operating activities for the six months ended December 31, 2020 increasedwas primarily due to an increase in operating earnings, which increased from $123.4$208 million in the corresponding prior-year period to $208.1$299 million for the six months ended December 31, 20202021, and a favorable impact from the timing of collection of trade receivables, which was partiallyprimarily offset by an unfavorable impact from inventory.the increase in contract assets.
Investing Activities
For the six months ended December 31, 2020,2021, cash used in investing activities was $354.4 million,$1.30 billion, compared to $199.2$354 million for the six months ended December 31, 2019.2020. The higher level of cash use was primarily driven by an increase in cash used in the acquisition of property, plant, and equipment, which totaled $338.9 million in the six months ended December 31, 2020 compared to $152.2 million for the six months ended December 31, 2019. The increase in acquisition of property, plant and equipmentinvesting activities was partially offsetprimarily driven by a decrease$1.00 billion increase in cash used for business acquisition activities.activities, partially offset by a $62 million decrease in cash used for purchases of property, plant, and equipment.
Financing Activities
For the six months ended December 31, 2020,2021, cash used inprovided by financing activities was $7.2 million,$1.03 billion, compared to cash used in financing activities of $101.8$7 million for the six months ended December 31, 2019. The decrease2020. Cash provided by financing activities was primarily driven by the $1.1 billion in net cash received from the issuance of the 2030 Notes and incurrence of our most recent tranche of term loans.
Cash used in financing activities isfor the six months ended December 31, 2020 was primarily driven by an annual installment on the deferred purchase consideration for the acquisition of Catalent Indiana, LLC and cash paid, in lieu of equity, for tax withholdings partially offset by the July 2020 exercise of an over-allotment option on 1.2 million additional shares by the underwriter onfor the equity offering in June 25, 2020, public offering of our Common Stock, resulting in net proceeds of $81.8 million for the six months ended December 31, 2020.$82 million.
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Guarantees and Security
The Senior Notes
All obligations under Operating Company's Euro 20282027 Notes, USD 2026 Notes, and U.S. dollar-denominated 5.00%2.375% euro-denominated senior notes due 20272028, 2029 Notes, and 2030 Notes (collectively, the "Senior 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. Each of the Senior Notes is separately guaranteed by all of Operating Company'sour wholly owned U.S. subsidiaries that guarantee the senior secured credit facilities. None of the Senior Notes is guaranteed by either PTS Intermediate Holdings LLC or Catalent, Inc.
Debt Covenants
Senior Secured Credit Facilities
The credit agreement governing Operating Company’s senior secured credit facilities (as amended, the “Credit Agreement”)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 indebtedness; and change Operating Company’sour lines of business.
The Credit Agreement also contains change-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, 2020, Operating Company was2021, we were in compliance with all material covenants under the Credit Agreement.
Subject to certain exceptions, the Credit Agreement permits Operating Companyus and itsour restricted subsidiaries to incur certain additional indebtedness, including secured indebtedness. None of Operating Company'sour non-U.S. subsidiaries or itsour Puerto Rico subsidiary is a guarantor of the loans.
Under the Credit Agreement, Operating Company'sour 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“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.
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
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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.
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The Senior Notes
The several indentures governing each series of the Senior Notes (collectively, 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; pay dividends on, repurchase, or make distributions in respect of their capital stock or make other 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 series of Senior Notes, or the applicable Trustee under the Indentures, may declare the applicable Senior Notes immediately due and payable; or in certain circumstances, the applicable Senior Notes will become automatically immediately due and payable. As of December 31, 2020,2021, Operating Company was in compliance with all material covenants under the Indentures.
Geographic Allocation of Cash
As of December 31, 20202021 and June 30, 2020,2021, our non-U.S. subsidiaries held cash and cash equivalents of $266.9$360 million and $228.0$351 million, respectively, out of the total consolidated cash and cash equivalents of $833.1$849 million and $953.2$896 million, respectively. These balances are dispersed across many locations around the world.

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. In April 2020,February 2021, we entered into anreplaced one interest-rate swap agreement with Bank of America N.A. with another, and each acts or acted as a hedge against the economic effect of a portion of the variable-interest obligation associated with our U.SU.S. dollar-denominated term loans under our senior secured credit facilities, so that the interest payable on that portion of the debt becomes fixed at a certain rate, thereby reducing the impact of future interest-rate changes on future interest expense. The applicable rate for the U.S. dollar-denominated term loan isunder the Credit Agreement was LIBOR (subject to a floor of 1.00%0.50%) plus 2.25%;2.00% as of December 31, 2021; however, as a result of entering into the current interest-rate swap agreement, the floatingvariable portion of the applicable rate on $500.0$500 million of the term loan is nowwas effectively fixed at 1.26% for a total fixed rate0.9985% as of 3.51%.February 2021.
Currency Risk Management
We are exposed to fluctuations in the euro-U.S. dollar exchange rate on our investments in our foreign 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, 2020,2021, we had $993.1$933 million of euro-denominated debt outstanding that qualifies as a hedge of a net investment in foreignEuropean operations. Refer to Note 10,Derivative Instruments and Hedging Activities, to our Consolidated Financial Statements for further discussion of net investment hedge activity in the period.
From time to time, we may use 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 use such contracts to protect the value of existing foreign currency assets and liabilities. Currently, we do not use any forward foreign currency exchange contracts. We expect to continue to evaluate hedging opportunities for foreign currency in the future.
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Contractual Obligations
The contractual obligations of the Company are set forth in Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations contained in our Fiscal 2020 10-K. Other than the contractual obligations noted below, there has been no material change to the disclosure presented in our Fiscal 2020 10-K. Refer to Note 6, Long-Term Obligationsand Short-Term Borrowings to our Consolidated Financial Statements for a further discussion regarding our long-term obligations.
(Dollars in millions)TotalFiscal 2021Fiscal 2022-Fiscal 2023Fiscal 2024-Fiscal 2025Thereafter
Venture capital investment commitments (1)
$11.5 $11.5 $— $— $— 
(1) The timing of the remaining capital commitment payments to venture capital funds is subject to the procedures of the limited liability partnerships and limited liability companies; the above table reflects the earliest possible date the payment can be required under the relevant agreements.

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 arrangement as of December 31, 2020.2021.

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ItemITEM 3.    QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
We are exposed to cash flowFor 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 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
We have historically used interest-rate swaps to manage the economic effectFiscal 2021 10-K. As 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.
In April 2020, we entered into an interest-rate swap agreement with Bank of America N.A. as a hedge against the economic effect of a portion of the variable-interest obligation associated with our U.S dollar-denominated term loans under our senior secured credit facilities, so that the interest payable on that portion of the debt becomes fixed at a certain rate, thereby reducing the impact of future interest-rate changes on future interest expense. The applicable rate for the U.S. dollar-denominated term loan is LIBOR (subject to a floor of 1.00%) plus 2.25%; however, as a result of entering into the interest-rate swap agreement, the floating portion of the applicable rate on $500.0 million of the term loan is now effectively fixed at 1.26%, for a total fixed rate of 3.51%.
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 translationalDecember 31, 2021, there has been no material change 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, and Brazilian real. 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, our functional currency. The financial statements of our operations outside the U.S. are measured using the local currency as the functional currency, except in Argentina. Adjustments to translate the assets and liabilities of these foreign operations in U.S. dollars are accumulated as a component of accumulated 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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ItemITEM 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 Chief Executive Officer and our Senior 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 of our Chief Executive Officer and our Senior 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 Chief Executive Officer and our Senior Vice President and Chief Financial Officer concluded that, as of December 31, 2020,2021, our disclosure controls and procedures were effective to accomplish their objectives at the reasonable assurance level.
Changes in Internal Control over Financial Reporting
During the three months ended December 31, 2020, there have beenThere was no changes in the Company’schange that materially affected, or is reasonably likely to materially affect, Catalent’s internal control over financial reporting that have materially affected, or are reasonably likely to materially affect, its internal control over financial reporting.occurred during the period covered by this Quarterly Report on Form 10-Q.
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PART II.    OTHER INFORMATION
ItemITEM 1.    LEGAL PROCEEDINGS
From time to time, we 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. We intend to vigorously defend ourselves against any such litigation and do not currently believe that the outcome of any such litigation will have a material adverse effect on our consolidated 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, we receive 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. We generally respond 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. We expect to incur costs in future periods in connection with future requests.
ItemITEM 1A.    RISK FACTORS
In addition to the other information set forth in this report, you should carefully consider the factors discussed in the section entitled Risk Factors“Risk Factors” in our Fiscal 20202021 10-K, which could materially affect our business, financial condition, or future results. The risks described in such report 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, or operating results.

Other than what was disclosed in the Special Note Regarding Forward-Looking Statements, there has been no material change to the risk factors disclosed in our Fiscal 20202021 10-K.
ItemITEM 2.    UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS

None.

Purchase of Equity Securities

None.

ItemITEM 3.    DEFAULTS UPON SENIOR SECURITIES

None.

ItemITEM 4.    MINE SAFETY DISCLOSURES

Not applicable.

ItemITEM 5.    OTHER INFORMATION
Not applicable.

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ItemITEM 6.    EXHIBITS
Exhibits:
Fourth Amended and Restated Certificate of Incorporation of Catalent, Inc., as filed with the Secretary of State of the State of Delaware on October 28, 2021 (incorporated by reference to Exhibit 3.1 to the Company’s Current Report on Form 8-K filed on November 2, 2021).
Bylaws of Catalent, Inc., effective October 28, 2021 (incorporated by reference to Exhibit 3.2 to the Company’s Current Report on Form 8-K filed on November 2, 2021).
  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. *
  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. *
  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. **
  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. **
101.1101  The following financial information from Catalent, Inc.’s Quarterly Report on Form 10-Q for the quarter ended December 31, 20202021 formatted in inline XBRL: (i) Consolidated Statements of Operations for the Three and Six Months Ended December 31, 20202021 and 2019;2020; (ii) Consolidated Statements of Comprehensive Income for the Three and Six Months Ended December 31, 20202021 and 20192020 (iii) Consolidated Balance Sheets as of December 31, 20202021 and June 30, 2020;2021; (iv) Consolidated Statement of Changes in Shareholders’ Equity as of December 31, 20202021 and 2019;2020; (v) Consolidated Statements of Cash Flows for the Six Months Ended December 31, 20202021 and 2019;2020; 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
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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 2, 20211, 2022By: /s/ Wetteny JosephRICKY HOPSON
 Wetteny JosephRicky Hopson
 Senior Vice President, & Chief FinancialAccounting Officer

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