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Akorn Operating Company LLC (Akorn Inc. prior to its bankruptcy) was an American generic pharmaceuticals manufacturer based in Lake Forest, Illinois. The company dealt in developing, manufacturing and marketing of generic and prescription drugs as well as animal and consumer health products.[1] It was a component of the NASDAQ Biotechnology Index.

Key Information

History

[edit]

John Kapoor is not the founder but has been a major shareholder since the 1990s.[2]

Akorn acquired rival Hi-Tech Pharmacal in 2013.[3]

In June 2015, it was reported that a hacker was trying to sell an Akorn customer database of more than 50,000 records. Akorn commented that "Although much of the information acquired is publicly available, we are in the process of notifying our valued customers about this incident".[4]

In April 2017, Akorn agreed to be acquired by Fresenius for $4.3 billion.[5] These plans were abandoned by Fresenius after Akorn couldn't meet basic requirements for an acquisition.[6]

In October 2018, Akorn received Abbreviated New Drug Application approval from the Food and Drug Administration for Bimatoprost Ophthalmic Solution, 0.03%.[7]

On May 21, 2020, Akorn filed for Chapter 11 bankruptcy and entered in to a Restructuring Support Agreement with lenders, which represents over 75 percent of its secured debt. The filing is to assist with an in-court sale of the company "while addressing litigation-related overhangs and best positioning the business for long-term success under new ownership".[8]

On September 14, 2022, Akorn was sued by the government for its pricings. Akorn paid $7.9 Million to "Resolve Allegations of Fraudulent Billing".[9]

On February 22, 2023, on a brief Teams call, Akorn CEO Douglas Boothe announced that the company had filed for Chapter 7 bankruptcy. All operations were ceased, and all employees were laid off, effective immediately. [10]

References

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Akorn

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Akorn Operating Company LLC, previously known as Akorn Inc., was an American pharmaceutical company headquartered in , focused on the development, manufacturing, and marketing of generic prescription , branded pharmaceuticals, over-the-counter medications, eye care products, and animal health solutions. The firm operated as a niche player in the generics sector, emphasizing sterile injectables, ophthalmics, and other specialized formulations, but faced mounting regulatory scrutiny and financial pressures, including FDA observations on manufacturing quality that derailed a proposed acquisition by Fresenius Kabi in 2018. These challenges led to a Chapter 11 bankruptcy filing in May 2020, followed by a Chapter 7 in February 2023, which shuttered all U.S. operations, eliminated its workforce, and triggered shortages of essential such as liquid albuterol and certain ophthalmic preparations. In its Chapter 7 proceedings, Akorn's assets, including approved drug applications, yielded approximately $309 million against $184 million in secured , underscoring the value of its amid operational collapse.

Overview

Founding and Corporate Structure

Akorn, Inc. was incorporated as a corporation in 1971 in Abita Springs, . The company operated as a specialty generic pharmaceutical manufacturer, structured primarily as a holding entity with multiple wholly-owned subsidiaries focused on development, manufacturing, and marketing activities. In 1997, Akorn relocated its corporate headquarters from to the , metropolitan area, later establishing its primary base in . Key U.S. subsidiaries included Advanced Vision Research, Inc. (), Akorn (New Jersey), Inc. (), and Akorn Animal Health, Inc. (), among others, which supported operations in generics, branded pharmaceuticals, and animal health products. Akorn functioned as a publicly traded entity on the under the ticker AKRX until its Chapter 11 bankruptcy filing in 2023, after which it reorganized as Akorn Operating Company LLC, a private entity. The corporate structure emphasized , with subsidiaries handling specialized functions such as formulation development and .

and Product Focus

Akorn, Inc. functioned primarily as a generic pharmaceutical manufacturer, emphasizing the development, production, and commercialization of multisource prescription drugs in specialized that presented manufacturing challenges for competitors. Its core strategy involved targeting niche markets with high , such as sterile injectables, ophthalmic solutions, oral liquids, topicals, and inhalation products, where complex formulations or delivery methods limited generic competition. This approach allowed Akorn to generate revenue through cost-effective replication of branded drugs post-patent expiration, focusing on therapeutic areas including , anti-infectives, and disorders. The company's product portfolio comprised over 140 generic and select branded offerings, with a significant emphasis on ophthalmics (e.g., hydrochloride solutions) and hospital-administered injectables (e.g., and hydrochloride). Animal health products, such as veterinary ophthalmics and injectables, formed a smaller but dedicated segment, marketed under the Akorn Animal Health brand. Akorn's revenue model relied heavily on the prescription pharmaceuticals division, which accounted for the majority of sales, derived from sales to wholesalers, hospitals, and pharmacies rather than channels. Inorganic expansion via acquisitions, licensing agreements, and technology transfers supplemented organic R&D efforts to broaden this portfolio. To streamline operations, Akorn periodically divested non-core assets, including its branded ophthalmic portfolio (seven products sold to Théa Open Innovation in January 2022 for an undisclosed sum) and over-the-counter consumer health lines (e.g., TheraTears, acquired by for $230 million in May 2021). These moves refocused resources on high-margin generics and animal care, aligning with a strategy of operational efficiency amid competitive pressures in the generics sector.

Key Facilities and Operations

Akorn maintained manufacturing facilities in multiple locations, primarily focused on producing generic pharmaceuticals, including sterile injectables, ophthalmics, topicals, and oral liquids. The site served as a key hub for sterile manufacturing and packaging of injectables and ophthalmics. The facility handled drug production, including sterile and non-sterile formulations. In , operations emphasized similar pharmaceutical manufacturing processes. Internationally, Akorn operated sites in Hettlingen, , for specialized production, and Paonta Sahib, , supporting expanded capacity. Corporate headquarters were located in , overseeing research, development, and administrative functions. These facilities enabled , from formulation to packaging, targeting niche markets like , antidotes, and products. In February 2023, Akorn Operating Company LLC filed for Chapter 7 bankruptcy, resulting in the cessation and shutdown of all manufacturing and operational activities across its facilities.

Historical Development

Inception and Early Expansion (1971–2000)

Akorn, Inc. was incorporated in in 1971 as a specialty pharmaceutical company initially focused on ophthalmic products, following its establishment by Joe Yazbeck in 1969. Headquartered in Abita Springs near New Orleans, the company began operations by developing and marketing generic and alternative , including ophthalmics and injectables, targeting niche markets in hospital and specialty drugs. Early growth was modest, emphasizing manufacturing capabilities for sterile injectables and ophthalmic solutions amid a competitive generic sector. Expansion accelerated in the late 1980s through strategic acquisitions to broaden product portfolios and expertise. In January 1988, Akorn acquired Spectrum Scientific Pharmaceuticals, Inc. for 187,000 shares of , enhancing its injectable offerings. This was followed by the September 1989 acquisition of Norbrook America, Inc. for one million shares, which was merged into a (Walnut Pharmaceuticals) and later sold in 1993. Additional purchases included the assets of Optometric Pharmaceuticals Inc. for $355,000 in 1990 and Taylor Pharmaceuticals for 926,000 shares in January 1992, bolstering ophthalmic and generic capabilities. In 1991, Dr. John N. Kapoor assumed the role of president, steering the company toward aggressive expansion and leadership in generic pharmaceuticals. By the mid-1990s, Akorn pursued further diversification. The July 1994 acquisition of the segment from Optical Radiation Corp.'s ophthalmic division, valued at 5.25 million shares, strengthened its surgical product line. In May 1996, it acquired Pasadena Research Laboratories, Inc. and secured rights to an injectable product line from Janssen Pharmaceutica NV for $1.6 million, alongside FDA approval for AK-T-Caine PF ophthalmic solution. The company relocated its corporate headquarters to the , area in 1997, facilitating proximity to larger markets and R&D hubs, and began marketing products such as Dehydrated Alcohol Injection, USP in 5 mL vials and Sulfate Injection, USP 50 mg/mL in 1 mL ampules that year. Revenue grew from $30 million in 1995 to $42 million in 1997, reflecting expanded operations. In July 1998, Akorn acquired Advanced Remedies, Inc. and launched a generic version of cromolyn sodium 4% ophthalmic solution, competing with branded products from and ; annual revenue reached $56.7 million, up 35% from the prior year. That November, Floyd Benjamin succeeded as president and CEO, with retaining the chairmanship. These moves positioned Akorn as a mid-sized player in generics by 2000, with facilities supporting sterile in and emerging Midwest operations.

Growth Phase and Acquisitions (2000–2010)

During the early 2000s, Akorn Inc. faced operational losses and financial pressures, reporting net losses from operations in 2000 through 2002 amid challenges in and market competition in generic pharmaceuticals. The company stabilized through strategic initiatives, including the formation of Akorn-Strides, LLC, a with Strides Arcolab Limited on September 22, 2004, in which Akorn held a 50% stake after each partner invested $1.5 million; this entity focused on developing and marketing generic injectable products for the U.S. market, contributing initial sales of $295,000 in 2008 and $10.91 million in 2009. Growth accelerated mid-decade via product launches and licensing agreements. On November 16, 2004, Akorn launched Calcium-DTPA and Zinc-DTPA injectables as orphan drug approvals for treating radioactive contamination, under a licensing deal with Hameln Pharmaceuticals (later terminated in 2009). In September 2007, the company entered the biologics and vaccines segment through a distribution agreement with Massachusetts Biologic Laboratories for Td vaccine, followed by flu vaccine sales generating $6.38 million in revenue in 2008. Akorn also launched Akten®, a topical ophthalmic anesthetic, in the fourth quarter of 2008. These efforts drove revenue expansion, with net sales rising 60% to $71.2 million in 2006 from 2005 levels, then surging 77% to $93.6 million in 2008 from $52.9 million in 2007, though dipping to $75.9 million in 2009 amid segment exits. Acquisitions remained limited, with no major company purchases recorded; instead, Akorn pursued product rights and partnerships, including an exclusive 2004 agreement with for oncology injectables, yielding three ANDA approvals by but no launches. By , the firm had secured 10 ANDA approvals and maintained a pipeline targeting a $1 billion addressable market, supported by a new R&D center opened in , on February 1, 2010. Leadership transitions in 2010, including Raj Rai as interim CEO, positioned Akorn for further expansion into niche generics. This phase marked a shift from earlier instability to revenue recovery and pipeline buildup, though without transformative mergers.

Peak Operations and Challenges (2010–2017)

During this period, Akorn pursued aggressive expansion through targeted acquisitions to bolster its generics, ophthalmics, and consumer health segments, driving substantial revenue growth. In 2011, the company acquired Advanced Vision Research for $26 million, adding over-the-counter eye care products with approximately $20 million in prior-year sales across domestic retail and international markets. Subsequent deals included assets from Kilitch Drugs () Limited in February 2012, enhancing injectable manufacturing capabilities, and Hi-Tech Pharmacal in 2014, which contributed $176.9 million in revenue and expanded branded and generic offerings. The January 2015 acquisition of Akorn AG's Swiss facility further diversified operations into European markets and sterile manufacturing. These moves aligned with Akorn's strategy of leveraging acquisitions for development and in high-margin areas like ophthalmics and injectables. Revenue reflected this expansion, rising from $86.4 million in 2010—marked by 81% growth amid increased product demand—to a peak of $1.1 billion in 2016, fueled by full-year impacts from recent acquisitions and organic sales in generics. reached $1.22 in 2015, up $1.09 from 2014, underscoring operational scale-up, including investments in R&D facilities to accelerate (ANDA) filings. By 2017, this trajectory culminated in a $4.3 billion merger agreement with Fresenius Kabi, valuing Akorn at $34 per share and signaling market confidence in its diversified portfolio of over 200 products. Notwithstanding growth, Akorn encountered early manufacturing and compliance hurdles that strained operations. An FDA inspection of its facility in September 2010 yielded a Form 483 citing observations on processes, though not escalating to a warning letter at the time. Integrating acquired assets, such as those from Hi-Tech and Akorn AG, introduced complexities in quality systems harmonization and alignment, amid competitive pressures in low-margin generics. These factors, while not immediately derailing expansion, highlighted vulnerabilities in scaling sterile and ophthalmic production, setting the stage for intensified scrutiny in subsequent years.

Regulatory and Compliance Issues

FDA Inspections and Data Integrity Problems

The U.S. (FDA) conducted inspections at Akorn's manufacturing facilities that uncovered significant deficiencies, including inaccurate record-keeping, potential data manipulation, and inadequate controls over systems, compromising the reliability of for products. These issues spanned multiple sites and involved failures to maintain complete, accurate records as required under current (CGMP) regulations, such as 21 CFR 211.188, which mandates that records include all from tests necessary for compliance. At the facility, an FDA inspection from April 9 to May 16, 2018, identified discrepancies in cleaning and sanitization records, such as documented cleanings that were not performed (e.g., for HCl lot 041328 on April 5, 2018) and undocumented interventions on the ISO 5 filling line. The subsequent warning letter, issued January 3, 2019, highlighted FDA concerns over the accuracy of intervention and sanitization records, noting risks of contamination from skipped steps with incomplete documentation. Laboratory controls were deficient, including unperformed impurity tests (L-Cystine and L-Cysteine) for injection stability samples since 2016, leading to a recall on June 22, 2018, due to unconfirmed specifications. Annual product review reports omitted critical changes, such as ceasing impurity testing and equipment modifications affecting eight products in 2017. A separate at the facility from July 23 to August 30, 2018, revealed more direct handling vulnerabilities, including the ability to delete or alter on instruments like FTIR, TOC, and analyzers due to inadequate computerized system controls and unrestricted administrator access. Over 294 injection sequences from January 2017 to August 2018 lacked required signatures, and out-of-specification (OOS) investigations were inadequate or prolonged, such as a 19-month delay in resolving impurity failures despite recalculations, and unaddressed root causes for osmolality issues in lot 6C95A. The warning letter issued June 13, 2019, stated that the system "does not adequately ensure the accuracy and integrity of to support the , effectiveness, and of the drugs you manufacture." These findings echoed prior violations at other Akorn sites, indicating persistent systemic failures in oversight. Such deficiencies raised broader concerns about the trustworthiness of Akorn's data, as FDA investigators noted that the extent of violations remained unknown, potentially affecting batch releases and product approvals. In one documented case tied to operations, employees reportedly rounded down test results for impurities to meet specifications, exemplifying deliberate manipulation uncovered during probes informed by FDA observations. Akorn's responses to these citations involved remediation plans, but FDA emphasized the need for comprehensive root-cause analysis and verifiable corrections to restore data reliability.

Warning Letters and Remediation Efforts

The U.S. Food and Drug Administration (FDA) issued a warning letter to Akorn, Inc. on February 4, 2019, citing significant violations of current good manufacturing practice (CGMP) regulations at its Decatur, Illinois facility, based on an inspection conducted there. The letter highlighted deficiencies including inadequate investigation of manufacturing discrepancies, failure to ensure data accuracy and reliability, and insufficient controls over computer systems, which echoed prior data integrity concerns identified during FDA audits starting in 2017. On June 13, 2019, the FDA issued another warning letter to Akorn for its facility, following an ending August 30, 2018, which identified repeat CGMP violations such as poor practices, inadequate , and data manipulation risks. The agency noted these issues persisted despite Akorn's prior awareness from earlier inspections, attributing failures to inadequate management oversight and quality unit effectiveness. In response to the February 2019 warning, Akorn committed to collaborating with the FDA, submitting detailed remediation plans that included enhanced training, process validations, and system upgrades to address and CGMP compliance gaps. For the June 2019 letter, the company outlined long-term measures such as procedural enhancements, management oversight improvements, and third-party audits, while the FDA acknowledged some initial corrective actions but deemed them insufficient to resolve systemic risks to product quality. Despite these efforts, subsequent FDA assessments indicated ongoing deficiencies, including unresolved repeat violations that posed potential risks.

Consequences for Manufacturing Quality

The U.S. Food and Drug Administration's (FDA) inspections of Akorn's facilities uncovered systemic deficiencies in manufacturing processes that compromised product quality, particularly at the plant. A Form 483 issued on May 16, 2018, following an ending that date, documented failures including inadequate procedures to prevent , poor where operators touched critical surfaces without proper intervention documentation, and non-integral materials allowing potential ingress of contaminants. These lapses indicated that batches produced under such conditions risked adulteration, as environmental controls and operator practices did not reliably ensure sterility or purity. Subsequent warning letters amplified these concerns, revealing data integrity failures that further eroded manufacturing reliability. The FDA's February 4, 2019 letter for the Decatur facility cited manipulated laboratory records to obscure out-of-specification results and undocumented interventions during production and sanitization, rendering historical manufacturing data unreliable for validating process controls or batch release decisions. Similarly, the June 13, 2019 letter for the facility highlighted inadequate investigations into equipment failures and sterility issues, such as leaky ophthalmic solutions attributed to supplier defects without sufficient root-cause or follow-up testing. Such practices meant that deviations in were not systematically addressed, perpetuating risks of substandard products and necessitating batch holds or reworking to meet current good manufacturing practice (CGMP) standards. These regulatory findings imposed direct operational constraints on Akorn's manufacturing quality. The FDA withheld approvals for new abbreviated new drug applications (ANDAs) and required comprehensive remediation plans, including overhauls and validations, estimated to exceed $40 million in costs by early 2019. Internal audits revealed ongoing uncorrected deficiencies, diverting personnel and capital from routine production enhancements to compliance efforts, which Akorn's 2018 third-quarter financials attributed to elevated operating expenses and erosion. Persistent failures, including unaddressed CGMP violations across sites, signaled a culture of inadequate quality oversight, as evidenced by FDA's assertion that Akorn's management bore responsibility for not ensuring thorough discrepancy investigations. In the aggregate, these consequences manifested as a degraded ecosystem incapable of sustaining consistent , with unverified processes leading to quantifiable output shortfalls—such as a sharp decline in sterile injectables production post-2017 inspections—and heightened risks for existing inventory. Although immediate production halts were not mandated, the regulatory scrutiny enforced voluntary batch quarantines and third-party validations, ultimately contributing to operational inefficiencies that foreshadowed Akorn's broader , where ceased entirely in February 2023 amid , triggering of over 70 products due to discontinued programs.

Merger Attempt with Fresenius Kabi

Agreement Terms and Initial Announcement

On April 24, 2017, Fresenius Kabi AG announced it had entered into a definitive merger agreement to acquire Akorn, Inc., a U.S.-based generic pharmaceutical manufacturer, in an all-cash transaction valued at $34 per share, representing an equity value of approximately $4.3 billion plus Akorn's net debt of about $450 million for an enterprise value of roughly $4.75 billion. The deal was approved unanimously by the boards of both companies and was projected to close in early 2018, subject to customary closing conditions including regulatory approvals and shareholder consent; it was expected to be accretive to Fresenius Kabi's net income and earnings per share in 2018, excluding integration costs. Under the terms of the Agreement and Plan of Merger dated April 24, 2017, a wholly owned of Fresenius Kabi (Merger Sub) would merge with and into Akorn, with Akorn continuing as the surviving entity and becoming a wholly owned of Fresenius Kabi. Each outstanding share of Akorn would be converted into the right to receive $34 in , without or dividends, while Akorn equity awards would generally vest and convert into equivalents at the same per-share price. The agreement included standard representations, warranties, covenants, and termination rights, including a material adverse effect () clause allowing Fresenius Kabi to terminate if Akorn suffered a general or breached certain quality and compliance representations, with Akorn facing a $225 million termination fee if Fresenius Kabi validly terminated on those grounds. The initial announcement highlighted strategic synergies, including expanded U.S. manufacturing capacity, a broadened portfolio, and enhanced sterile injectable capabilities for Fresenius Kabi, while providing Akorn shareholders with a 34% premium over the unaffected 30-day volume-weighted average share price prior to media reports of acquisition interest. Akorn's shareholders subsequently approved the merger on , 2017, with 83.9% of outstanding shares voted in favor.

Due Diligence Discoveries

During post-signing due diligence, Fresenius Kabi identified pervasive failures at Akorn's manufacturing facilities, particularly in , and . FDA inspections in December 2017 and February 2018 issued Form 483 observations citing deliberate falsification of laboratory test results, including backdating data entries and excluding out-of-specification results from batch records to conceal non-conformities. Akorn's internal remediation efforts, prompted by whistleblower complaints received by Fresenius in early 2018 alleging systemic manipulation of quality control data, confirmed instances of employee misconduct, such as supervisors directing technicians to alter entries in electronic systems. These revelations contradicted Akorn's pre-merger representations of and operational integrity. Financial performance metrics uncovered during showed a sharp deterioration disproportionate to industry trends. Akorn's net product declined 34% year-over-year in the fourth quarter of 2017, dropping from $247 million to $163 million, with adjusted EBITDA turning negative at -$4.7 million compared to a $40 million profit the prior year. Projections indicated sustained losses, with full-year net forecasted at $620–$640 million, a 30% reduction from 2017, amid customer losses and pricing pressures not offset by Akorn's limited diversification as a generics-focused entity. The later determined these combined regulatory and financial issues constituted a material adverse effect under the merger agreement, validating Fresenius's termination on April 22, , as the problems were neither short-duration nor industry-wide. Fresenius's investigations also highlighted Akorn's inadequate response to FDA concerns, including delays in disclosing inspection findings and incomplete cooperation on remediation covenants, breaching interim operating obligations. Independent expert testimony during litigation affirmed that the data falsifications risked widespread product recalls and supply disruptions, eroding Akorn's core value as a low-cost generics . These discoveries shifted Fresenius's assessment from the initial view of Akorn's "generally good regulatory standard" to recognition of fundamental operational defects.

Litigation Outcome and Termination

Fresenius Kabi AG announced the termination of the merger agreement with Akorn, Inc. on April 22, 2018, citing Akorn's failure to satisfy closing conditions, including breaches of representations and covenants related to and ordinary course operations, as well as the occurrence of a . The termination was based on revelations of widespread failures at Akorn's manufacturing facilities, including FDA findings of falsified test results and manipulated stability data, which Akorn had misrepresented in its signing-date representations. Akorn filed suit in the on April 23, 2018, seeking to compel Fresenius to close the merger and alleging that Fresenius had materially breached the agreement through inadequate efforts. In a ruling on October 1, 2018, Andre Bouchard held that Fresenius validly terminated the agreement on multiple independent grounds: Akorn's inaccurate representations about constituted a material breach; Akorn failed to conduct its business in the ordinary course, evidenced by operational disruptions and executive departures; and an had occurred due to the regulatory issues' projected long-term impact on Akorn's earnings, estimated at over 20% duration materiality under the agreement's definition. The court rejected Akorn's counterclaims, finding no material breach by Fresenius and emphasizing that the MAE clause's high bar was met given the qualitative severity of Akorn's compliance failures, which undermined its core manufacturing value. Akorn appealed to the , arguing errors in the Chancery Court's interpretation of the provision and breach findings. On December 7, , the affirmed the Chancery decision in a per curiam order, upholding the termination without altering the lower court's analysis and confirming that Akorn's regulatory violations and financial deterioration justified invoking the and other termination rights. This outcome marked the first instance in Delaware where a buyer successfully terminated a merger solely on an MAE basis, setting a that regulatory non-compliance can trigger such clauses when reasonably expected to impair long-term value, though the bar remains exceptionally high for short-term or industry-wide effects. The litigation effectively ended the $4.75 billion deal, with no further appeals pursued, leaving Akorn to face independent financial and regulatory pressures.

Financial Decline and Bankruptcy

Pre-Bankruptcy Financial Strains

Akorn faced mounting financial difficulties in the period following its 2020 Chapter 11 restructuring, including chronic operating losses, elevated leverage, and constrained liquidity that hindered remediation efforts and business continuity. Lenders had acquired the company during the 2020 proceedings to avert , but persistent burdens—stemming from FDA-mandated facility upgrades and fixes—drained cash reserves without commensurate revenue recovery. Debt levels remained burdensome, with secured obligations totaling approximately $184 million by early 2023, while adjusted debt-to-EBITDA ratios were projected to surpass 10x by year-end 2022 according to , driven by high remediation costs and subdued earnings from sales. highlighted Akorn in December 2022 as among 34 U.S. healthcare firms vulnerable to default, citing excessive indebtedness alongside weak operating metrics and shortfalls. A process initiated in failed to attract bids adequate to satisfy claims and liabilities, as potential buyers balked at the capital-intensive path to FDA compliance and the generics sector's razor-thin margins. Additional strains arose from a $7.9 million settlement in April over allegations of improper Medicare reimbursements for certain generics, further eroding financial stability amid broader industry pressures from pricing erosion in low-margin products. Unable to secure fresh capital or financing, Akorn's viability eroded, setting the stage for operational shutdown.

Chapter 11 Filing and Restructuring Attempts

Akorn, Inc. and 16 affiliated entities filed voluntary petitions for Chapter 11 bankruptcy protection on May 20, 2020, in the United States Bankruptcy Court for the District of (Case No. 20-11177). The filing followed prolonged financial pressures, including the failed merger with Fresenius Kabi and ongoing regulatory challenges, with the company seeking to deleverage its balance sheet and pursue strategic alternatives. In conjunction with the petitions, Akorn entered a Restructuring Support Agreement (RSA) with lenders holding over 75% of its approximately $290 million in secured , committing to support a recapitalization that would convert to equity and provide debtor-in-possession (DIP) financing of up to $135 million to sustain operations. The debtors proposed a Modified Joint Chapter 11 Plan of Reorganization, filed on June 30, 2020, which classified creditors into eight classes and impaired five, including secured lenders in Class 3. Under the plan, pre-petition secured lenders would receive 100% of the equity in the reorganized company, subject to dilution by a potential rights offering or sale proceeds, while general unsecured creditors were to receive distributions from retained litigation claims and other recoveries. The restructuring incorporated a process for a going-concern sale, though no qualified bids materialized beyond the lenders' credit bid, leading to the plan's reliance on internal recapitalization rather than an external transaction. Akorn continued normal operations during the proceedings, fulfilling obligations to customers and suppliers, with court approval for the DIP financing ensuring liquidity. The bankruptcy court confirmed the plan on September 1, 2020, following hearings that addressed objections from parties like the 1199SEIU Health Care Employees Union, which appealed the classification and treatment of claims but was ultimately unsuccessful. Effective October 1, 2020, the reorganized emerged from Chapter 11 with approximately $300 million in debt eliminated and secured lenders as the new owners, aiming to stabilize finances and address compliance issues. However, persistent operational and regulatory hurdles post-emergence underscored limitations in the restructuring's long-term viability.

Conversion to Chapter 7 and

Following the confirmation of its Chapter 11 reorganization plan in September 2020, which transferred ownership to pre-petition secured lenders, Akorn continued to grapple with persistent regulatory violations, deficiencies, and inability to secure new financing or viable buyers. By early 2023, failed marketing efforts for the business—hampered by government pricing liabilities and lack of appropriate bids—rendered ongoing operations unsustainable. On February 23, 2023, Akorn Operating Company LLC and two affiliates voluntarily filed petitions for relief under Chapter 7 of the Code in the U.S. Bankruptcy Court for the District of , transitioning the remnants of the company into proceedings with reported debts exceeding $100 million. This filing triggered an immediate cessation of all U.S. operations, including the shutdown of four facilities and the termination of the entire , such as approximately 400 employees at the plant. George L. Miller was appointed as the Chapter 7 to oversee the orderly of assets. The process focused on monetizing and other holdings, ultimately recovering $309 million from Abbreviated New Drug Applications (ANDAs) and related assets to address $184 million in secured debt, yielding higher recoveries than the prior Chapter 11 sale processes due to improved market conditions for generics assets. Pre-petition term loans from the 2020 restructuring, originally totaling $861.7 million, were among the obligations subordinated in the wind-down. The proceedings also prompted voluntary recalls of numerous products still within expiry, as the company ceased quality monitoring and distribution capabilities. A worker alleged violations of federal WARN Act requirements for plant closures and mass layoffs.

Controversies and Criticisms

Allegations of Data Falsification and Fraud

In early 2018, during due diligence for the proposed $4.3 billion merger with Fresenius Kabi AG—announced on April 24, 2017—Fresenius discovered evidence of falsified data in Akorn's submissions to the U.S. Food and Drug Administration (FDA). Akorn's Executive Vice President for Global Quality Affairs, the head of its quality function, had directed employees to fabricate stability testing data for an Abbreviated New Drug Application (ANDA) for azithromycin extended-release suspension since 2012, with similar manipulations affecting at least five other ANDAs. Fresenius publicly alleged that these actions represented "blatant fraud at the very top level" of Akorn's operations, rendering Akorn's representations about regulatory compliance untrue and requiring years of remediation for core business functions. Akorn responded by conducting an internal investigation, confirming the falsification of data in the implicated ANDAs, terminating the involved executive on March 22, 2018, and notifying the FDA of the issues. The company asserted that none of the six affected products had been marketed and that the problems were isolated, rejecting Fresenius's characterization of systemic fraud. However, Akorn's handling of related whistleblower complaints—received as early as alleging data manipulation in product development—drew criticism for inadequate follow-up, including reliance on narrow third-party audits that failed to uncover broader issues. FDA inspections substantiated and expanded on these concerns. At Akorn's facility (inspected April 9 to May 16, 2018), investigators identified failures to maintain accurate records of interventions and sanitization on aseptic filling lines, alongside broader deficiencies in ensuring for drug safety and quality; a warning letter issued on February 4, 2019, demanded a comprehensive remediation plan, including risk assessments for falsified or unreliable data. A subsequent inspection at the plant (July 23 to August 30, 2018) revealed chemists with unrestricted access to alter data on instruments like FTIR spectrometers and particle counters, deletion of audit trails, over 1,000 unsigned injection sequences from 2017–2018, and unjustified invalidation of out-of-specification results via unapproved "trial injections"; the FDA's June 13, 2019 warning letter concluded that these systemic lapses indicated unknown extents of data manipulation, posing risks to . An FDA Form 483 from the inspection, issued in November 2018, specifically cited employees rounding down impurity test results to meet specifications. In Akorn, Inc. v. Fresenius Kabi AG (, decided September 25, 2018), the court ruled that the "serious problems," including deliberate falsification of test results and inadequate controls, constituted a material adverse effect under the merger agreement, justifying Fresenius's termination on April 22, 2018. The opinion highlighted Akorn's submission of false data to the FDA and failure to conduct thorough investigations into lapses, affirming Fresenius's findings of pervasive regulatory non-compliance despite initial assurances. This decision, upheld by the in December 2018, marked the first judicial validation of a merger termination based on such -related .

Impact on Patients and Drug Shortages

Akorn's conversion to Chapter 7 in May 2023, following its initial Chapter 11 filing on February 22, 2023, resulted in the abrupt shutdown of all U.S. manufacturing operations, halting production and distribution of over 100 products. This closure immediately disrupted supply chains for essential medications, contributing to at least 14 drugs entering shortage status within a month and four others being discontinued. Patients faced reduced access to critical generics, including liquid albuterol—one of only two U.S. suppliers for this hospital-used bronchodilator for respiratory distress—and pediatric formulations, leading to rationing in emergency departments and pediatric wards. Antimicrobials like amoxicillin, chemotherapies for ovarian and bladder cancers, and ophthalmic agents such as phenylephrine, atropine, and fluorescein were also affected, delaying treatments and requiring clinicians to seek costlier alternatives or compound substitutes. In April 2023, Akorn issued a voluntary nationwide recall of all remaining human and animal drug products within expiry due to the shutdown, further exacerbating scarcity for ongoing therapies. The liquidation intensified existing vulnerabilities in the market, where low profit margins had already thinned manufacturer numbers, prompting hospitals to implement conservation protocols and divert resources to mitigate risks like treatment delays for antidotes and other niche therapies. This episode highlighted patient-level harms, including potential increases in adverse outcomes from suboptimal substitutions, amid a 2023 peak in U.S. shortages tracked by health-system pharmacists.

Shareholder and Stakeholder Lawsuits

Following the Delaware Chancery Court's September 2018 ruling permitting Fresenius Kabi AG to terminate its $4.75 billion merger agreement with Akorn due to material adverse effects from data integrity failures and regulatory non-compliance, Akorn's stock price plummeted by approximately 57% on October 1, 2018. This decline prompted a federal securities class action lawsuit filed by shareholders, alleging that Akorn and its executives violated federal securities laws through materially false and misleading statements about the company's FDA compliance, manufacturing quality systems, and ANDA submission processes. Plaintiffs claimed these misrepresentations artificially inflated Akorn's stock price, causing losses when corrective disclosures revealed pervasive data falsification and inspection failures at facilities in Decatur, Illinois, and Somerset, New Jersey. In August 2019, Akorn reached a tentative $74 million settlement with the shareholder class, which the company recorded as a charge against earnings in the second quarter of that year, without admitting wrongdoing. The settlement addressed claims stemming from two key corrective disclosures: one in December 2017 acknowledging FDA observations of data manipulation, and another in early 2018 tied to ongoing quality control deficiencies that undermined ANDA approvals. Final court approval followed, compensating affected shareholders for alleged damages from the stock's decline amid revelations of systemic operational flaws. Separately, during the merger proxy phase in 2017-2018, six Akorn shareholders initiated lawsuits in the U.S. District Court for the Northern District of Illinois, challenging the adequacy and completeness of disclosures in Akorn's preliminary regarding findings and regulatory risks. These actions were voluntarily dismissed as moot after Akorn amended its proxy disclosures and agreed to pay plaintiffs' attorneys $322,500 in fees, a practice common in merger-related litigation to expedite resolutions. However, in March 2025, the district court ordered the return of these fees, ruling the suits lacked merit and constituted improper "strike suits" under securities laws and Rule 11, with potential sanctions hinted for the filing firms, which had pursued similar actions in over 100 other mergers. No major lawsuits from non-shareholder stakeholders, such as , employees, or suppliers, were identified in connection with Akorn's Chapter 11 filing in May 2020 or its conversion to Chapter 7 in February 2023, though proceedings prioritized secured recoveries from asset sales totaling $309 million against $184 million in . Government actions, including a September 2022 DOJ settlement for false Medicare claims related to mislabeled products, involved regulatory penalties rather than private stakeholder litigation.

Legacy and Industry Impact

Asset Sales and Post-Liquidation Developments

Following the conversion to Chapter 7 liquidation on February 23, 2023, the bankruptcy trustee facilitated the sale of Akorn's assets, with a primary focus on its Abbreviated New Drug Applications (ANDAs) and related to maximize value amid ongoing drug shortages. The process yielded approximately $309 million in recoveries from these and other assets, surpassing the $184 million in secured debt obligations and demonstrating higher value extraction than Akorn's prior Chapter 11 proceedings. Sales were executed through multiple transactions, including 13 negotiated asset purchase agreements approved via 21 individual court orders, enabling swift transfer to operational buyers capable of resuming production. This approach prioritized urgency to restore supply chains for generic pharmaceuticals, with the American Bankruptcy Institute recognizing the transactions as the 2023 Asset Sale of the Year for their efficiency in a distressed scenario. One notable asset disposition involved Akorn's manufacturing facility, acquired in July 2023 by Rising Newco—a of Rising Pharmaceuticals—for $1.25 million. Rising Pharmaceuticals commenced commercial operations at the site by September 2023, focusing on sterile product manufacturing and packaging to address gaps left by Akorn's shutdown, which had idled the plant and contributed to shortages of hospital generics. Such transfers exemplified how sales mitigated broader supply disruptions, as buyers integrated Akorn's ANDAs to restart production of essential drugs like injectables and ophthalmics previously affected by Akorn's regulatory and financial failures. Post-liquidation developments included resolutions of lingering disputes, such as an August 2024 settlement between the estate and resolving a $28 million claim related to pre-bankruptcy transactions. The case remains active, with a June 2024 motion to convert back to Chapter 11 for structured liquidation pending, alongside scheduled omnibus hearings extending into September 2025 to oversee final distributions and claims. These proceedings underscore the challenges of unwinding a generic drugmaker's estate, where asset values hinged on transferable approvals amid liabilities like $80 million in pricing obligations that deterred whole-company bids. Overall, the sales preserved some industry capacity, though full restoration of Akorn's output has proven uneven due to the fragmented nature of the transfers.

Broader Lessons for Generic Drug Manufacturers

Akorn's downfall underscores the critical necessity for manufacturers to prioritize in all regulatory submissions and manufacturing processes. FDA inspections at Akorn's facilities revealed widespread falsification of laboratory records and stability , leading to warning letters in 2019 and subsequent revocation risks for multiple Abbreviated New Drug Applications (ANDAs). These violations not only triggered the collapse of its $4.3 billion merger with Fresenius Kabi in —Delaware's first court ruling allowing termination under a material adverse effect clause due to regulatory non-compliance—but also eroded market confidence and revenue streams. Generic firms operating in low-margin environments must implement robust, auditable systems to mitigate such risks, as shortcuts in documentation or testing can cascade into total loss of product approvals and operational viability. The case illustrates the perils of underinvesting in manufacturing infrastructure amid competitive pricing pressures. Akorn's repeated (CGMP) deficiencies, including inadequate and equipment maintenance, compounded financial strains from generic price erosion and disruptions. By 2023, conversion from Chapter 11 to Chapter 7 yielded $309 million from ANDA sales against $184 million in secured debt, highlighting that prolonged restructuring attempts may fail when core assets like manufacturing sites are irreparably tainted by regulatory scrutiny. Manufacturers should conduct regular internal audits and contingency planning for FDA enforcement actions, recognizing that generic markets' reliance on a few players amplifies the fallout from any single firm's non-compliance. Akorn's liquidation exacerbated shortages of over 70 generic drugs, including essential antibiotics and therapies, revealing systemic vulnerabilities in the U.S. generic where production is concentrated among cost-driven operators. This event prompted industry calls for diversified sourcing and incentives for domestic resilience, as rock-bottom discourages reinvestment in and capacity. Firms must balance aggressive cost controls with sustainable compliance investments to avert similar disruptions, which not only affect patient access but also invite heightened FDA oversight across the sector.

Economic and Supply Chain Ramifications

Akorn's liquidation under Chapter 7 bankruptcy led to the abrupt shutdown of all U.S. manufacturing facilities and the termination of its entire domestic workforce, totaling approximately 2,200 employees as of late 2022. In Decatur, Illinois, the company's primary production hub, over 400 workers were laid off effective immediately on February 22, 2023, without severance. Additional layoffs included 303 employees at the Amityville, New York, site, contributing to localized economic strain in manufacturing-dependent communities reliant on pharmaceutical jobs. Financially, the collapse erased substantial shareholder value, with Akorn's declining from roughly $4 billion in 2017 to $28 million by early 2020 amid regulatory and operational challenges. The Chapter 7 process recovered $309 million through sales of Abbreviated New Drug Applications (ANDAs) and related , exceeding the $184 million in secured claims and providing modest recovery for priority stakeholders. However, unsecured creditors and equity holders received negligible distributions, underscoring the risks of distress in the low-margin generic sector where razor-thin erodes profitability. Akorn's exit disrupted supply chains for generic injectables, ophthalmics, and oral liquids, niches where it held notable shares such as 3.44% of concentrated albuterol supply. The closure eliminated domestic production capacity for drugs where Akorn provided 100% of U.S. supply, forcing reliance on strained alternatives and amplifying shortages across hospital therapeutics like chemotherapies and antibiotics. This ripple effect burdened wholesalers and providers with inventory discards of Akorn products—deemed unusable post-recall—and heightened vulnerability in a consolidated generics market already pressured by single-source dependencies. While the Decatur facility later reopened under new ownership in late 2023, initial gaps underscored systemic fragilities, including underinvestment in backups amid competitive pricing wars.

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