|Public (under Dutch law)|
|Fate||merged with Upjohn to form Viatris|
|Founded||1961White Sulphur Springs, West Virginia, United Statesin|
|Heather Bresch, CEO|
|Products||Generic and specialty pharmaceuticals and active pharmaceutical ingredients|
|Revenue||US$11.434 billion (2018)|
|US$906 million (2018)|
|US$353 million (2018)|
|Total assets||US$32.735 billion (2018)|
|Total equity||US$12.167 billion (2018)|
Number of employees
|~35,000 (December 2018)|
|Footnotes / references|
Mylan N.V. was a global generic and specialty pharmaceuticals company domiciled in the Netherlands, with principal executive offices in Hatfield, Hertfordshire, UK and a "Global Center" in Canonsburg, Pennsylvania, US. In 2007, the company acquired a controlling interest in India-based Matrix Laboratories Limited, a top producer of active pharmaceutical ingredients (APIs) for generic drugs, and the generics business of Germany-based Merck KGaA. Through these acquisitions, the company grew from the third-largest generic and pharmaceuticals company in the United States to the second-largest generic and specialty pharmaceuticals company in the world.
The company develops and produces medicines for a wide range of medical disciplines, including oncology, anaphylaxis, antiretrovirals, cardiovascular, respiratory, dermatology, immunology, anesthesia and pain management, infectious disease, gastroenterology, diabetology/endocrinology, and women's healthcare.
In 2016, the company's pricing of the EpiPen, an epinephrine autoinjector, became controversial and was widely referred to as "price gouging". As a result, investigations were opened into whether the company had misclassified the EpiPen under the Medicaid Drug Rebate Program, a common form of pharmaceutical fraud. In October 2016, the company settled these investigations with the U.S. Department of Justice, agreeing to pay $465 million and enter into a corporate integrity agreement concerning the rebate program.
In a report published on June 12, 2017 Institutional Shareholder Services criticized the company for the "outsized compensation" of its directors. Former CEO Robert Coury received a $98 million 2016 pay package in spite of shareholder losses and the perceived harm to the company inflicted by the EpiPen controversies. The report urged the company's shareholders to oust all of the existing directors.
The company operates several divisions and subsidiaries in various regions around the world:
North & South America
- Mylan Pharmaceuticals, based in Morgantown, West Virginia
- Mylan Pharmaceuticals ULC, based in Etobicoke, Ontario
- Mylan LLC, based in Caguas, Puerto Rico
- Mylan Technologies Inc. (MTI) - transdermal drug delivery systems (TDDS) and related technologies based in St. Albans, Vermont
- UDL Laboratories Inc. based in Rockford, Illinois
- Somerset Pharmaceuticals Inc., a research and development company based in Tampa, Florida, owned by Mylan. Somerset develops Emsam, manufactured by Mylan Technologies and marketed in the United States by Dey, later renamed Mylan Specialty
- Mylan Laboratories Limited, based in Campos dos Goytacazes, Brazil
Oceania & parts of Asia
- Mylan New Zealand Limited, based in Auckland, New Zealand
- Mylan Laboratories Limited - headquartered in Hyderabad, India and operates approximately a dozen manufacturing facilities located in India and China
- Mylan Seiyaku Ltd. based in Tokyo, Japan
- Alphapharm, based in Australia
- Agila Specialties Pvt. Ltd. based in Bangalore, Karnataka, India
- OncoTherapies Ltd. based in Bangalore, Karnataka, India
Europe, Africa and West Asia
- Divisions under the Mylan name in Republic of Ireland, Austria, Belgium, the Czech Republic, Denmark, Finland, France, Germany, Hungary, Italy, the Netherlands, Norway, Poland, Portugal, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, and the United Kingdom.
- Arcana Arzneimittel GmbH based in Germany
- Generics Pharma Hellas based in Greece
- Gerard Laboratories based in Ireland
- Docpharma - generic pharmaceutical distribution company based in Belgium, the Netherlands and Luxembourg
Founded in 1961, the company was first located in an abandoned skating rink in White Sulphur Springs, West Virginia. The facility was moved to Pennsauken, New Jersey in 1962, to Princeton, West Virginia in 1963, and then Morgantown, West Virginia, in 1965, and in 1976 it relocated its corporate headquarters to the Pittsburgh suburb Canonsburg, Pennsylvania. Finally in 2004 it moved to a new office center in nearby Southpointe, a suburban business park located in the Pittsburgh suburb of Cecil Township, where it is still located.
Founding to 1980
Mylan Pharmaceuticals was founded as a drug distributor in 1961 by Milan Puskar and Don Panoz. In 1966, the company began manufacturing penicillin G tablets as well as vitamins and other dietary supplements.
Panoz left the company in 1969 and Puskar quit the company in 1973, as it grew and experienced financial difficulties. The board hired Roy McKnight as board chairman, who convinced Puskar to return in 1976.
With the passage of the Hatch-Waxman Act in 1984, the company and other small generic companies gained value; in the eighteen months following passage of the law the company's earnings grew 166% to $12.5 million and its stock value rose 800%.
Dyazide & Maxzide
In the 1980s one of the most prescribed drugs in the US was Dyazide, a diuretic that was a combination drug containing triamterene and hydrochlorothiazide; it had been on the market since 1965 and its patents had expired in 1980. Complications arose with the introductions of generics versions, because the formulation of Dyazide resulted in variable batches that made it impossible for generic manufacturers to show that their versions were bioequivalent.
Some generic companies committed fraud trying to bring a generic version of Dyazide. Bolar Pharmaceutical had the first generic version approved in 1987, but it turned out that Bolar had fraudulently substituted Dyazide for its own version to conduct studies that were submitted to the FDA. By 1989 the FDA rescinded its approval based on its suspicions and filed criminal charges against Bolar, to which Bolar eventually pled guilty in 1991.
The company chose to develop a new version of a triamterene/hydrochlorothiazide combination drug instead of going the generic route; it developed a different, more stable formulation and used different dosages of each active ingredient (50 mg hydrochlorothiazide and 75 mg triamterene, compared with Dyazide's 25 mg hydrochlorothiazide and 50 mg triamterene). This drug had to get approval as a new drug, as opposed to a generic. Their product was called Maxzide and was approved in 1984. The higher dose allowed once per day dosing, which the company and its marketing partner, Lederle, believed would help it compete against Dyazide, which had $210M in sales in 1983. However, the company's patents on the drug were declared invalid in court, and its marketing exclusivity expired in 1987, prompting a rush of generic competition
The company had concerns about the practices of its competitors and the FDA in general, and also with regard to companies seeking to bring generic versions of Maxzide. The company hired private investigators to examine its competitors' practices, and when it found evidence of corruption, it submitted it to the House Oversight and Investigations Committee, which investigated and found fraud and corruption within the Food and Drug Administration's generic drugs division and at other generic companies. Two of the companies that had gotten approval to market generic versions of Maxzide, Vitarine Pharmaceutical and Par Pharmaceutical, were targets of the company's initial investigation and were found to have used Maxzide to obtain their bioequivalence data, leading both companies to withdraw its generic competitor to Mylan's product.
The corruption in the nascent generics industry and at the office in the FDA regulating it was widely covered in the media, and led to widespread concern among doctors and the public in the late 1980s and early 1990s that generic drugs were not really the same as the branded drugs they were meant to replace.
In 1987, the company entered into a joint venture with Bolar to buy Somerset Pharmaceuticals; Mylan wanted access to Somersets' drug discovery capabilities as well as its new drug for Parkinson's, selegiline; the deal was completed in 1988 but its consummation was dependent on FDA approval of selegiline, which came in 1989.
The company acquired Bertek Inc. in 1993 for its transdermal patch technologies, and kept it as a subsidiary. In 1999, the company renamed Bertek as Mylan Technologies Inc. (MTI). MTI eventually came to be the contract manufacturer for the selegiline transdermal patch and was the first company to market generic nitroglycerin, estradiol, clonidine, and fentanyl transdermal patches.
In 1998 when it was the world's second largest generics company, the company came under investigation from the Federal Trade Commission after it raised the prices of its products, tripling them in the case of lorazepam. The company had entered into an exclusive agreement with Profarmica, an Italian company that supplied drug ingredients, after which the company's competitors had higher prices and a diminished supply of raw ingredients for lorazepam and other drugs. Before the round of price increases the price of generic drugs had been 5 - 10% of the price of branded drugs and afterwards it was around 50%. The FTC filed suit at the end of 1998 and 32 states filed parallel actions. The case was settled in 2000, with the company paying a total of $147M -- $100M in disgorged profits into a fund to reimburse consumers and state agencies that had overpaid, $8 million in attorney's fees to the State Attorneys General, $35 million, plus $4 million in attorney's fees, to settle certain class actions with insurers and managed care organizations—and Mylan and three ingredient suppliers (Cambrex Corporation, Profarmaco S.R.L., and Gyma Laboratories) also agreed to an injunction barring them from entering into similar anticompetitive agreements in the future.
Attempted King Pharmaceuticals acquisition
In 2004, the company and King Pharmaceuticals began discussing a deal in which Mylan would acquire King for $4 billion; Mylan wanted to expand its presence in branded pharmaceuticals and to acquire King's sales force. The deal was complicated by a number of factors, and included an SEC investigation into King's accounting and Carl Icahn obtaining a 9.8% interest in Mylan and becoming its largest stakeholder in order to kill the deal. The parties called off the deal in February 2005. Afterwards, Icahn offered to buy Mylan for $5.4B and nominated a slate of board members to change the direction of Mylan; he won three seats in May 2005. In June, the company bought back 25% of its shares in order to fend off Icahn. In July Icahn gave up his bid and sold his shares.
In October 2007, the company acquired the genetics division of Merck KGaA for $6.6 billion. The company acquired the rights to market the EpiPen in the transaction. At that time annual sales were around $200 million and the EpiPen had about 90% of the market.
In 2009, the company filed two lawsuits against the Pittsburgh Post-Gazette after the newspaper ran an article that was critical of the quality control procedures used at the company's Morgantown plant. The company had earlier quality control issues involving the FDA. The lawsuits were dropped in 2012 without any damages paid by the Post-Gazette, which stated "The Post-Gazette did not find and did not intend to report that Mylan had manufactured or distributed any defective drugs. The Post-Gazette regrets if any reader of the article thought otherwise."
Also in 2009, the company and its subsidiary UDL agreed to pay $118 million to settle a suit filed under the False Claims Act in which Mylan/UDL and two other companies were accused of underpaying states under the Medicaid Drug Rebate Program. The program requires drug companies to give rebates to states under Medicaid and the rebates are higher for new drugs than for generics; the suit said that the companies sold new drugs but paid rebates as if they were generics.
Generic Advair agreement
In 2011, the company entered into an agreement with Pfizer for the exclusive worldwide rights to develop, manufacture and commercialize Pfizer's generic equivalent to GlaxoSmithKline's Advair (US)/Seretide (UK) Diskus incorporating Pfizer's proprietary dry powder inhaler delivery platform. The company launched the product in the UK in 2015 and in February 2016 the FDA accepted its ANDA, putting it in line behind Hikma and Sandoz to launch a generic version in the US.
In 2012, the company launched a program called EpiPen4Schools to sell EpiPens in bulk and with discounts to schools. To participate in the program schools had to agree not to buy epinephrine autoinjectors from any other company for a year, a requirement which a company spokesperson said is no longer part of its program.
In December 2012, the National Association of State Boards of Education launched a policy initiative designed to "help state boards of education as they develop student health policies regarding anaphylaxis and epinephrine auto-injector access and use," and advocated for state laws protecting school from legal liability for stocking and using epinephrine autoinjectors. Gayle Manchin, the mother of the company's CEO, Heather Bresch, had become president of the association in 2010, and shortly after had discussed donations from her "daughter's company" to the association. Manchin had been appointed to the West Virginia state school board by her husband, then-governor of the state Joe Manchin, in 2007. In a statement, the company said, "There is no truth to the suggestion that the company's efforts were anything but straightforward or that we are aware of anyone advocating inappropriately for the right of schoolchildren to have access to potential life-saving medicine."
After successful lobbying from the company, in 2013, the "School Access to Emergency Epinephrine Act" became law after passing Congress with broad and bipartisan support; it protected anyone from liability if they administered epinephrine to a child in a school (previously, only trained professionals or the affected person were allowed to administer the drug, and were open to liability), and it provided some financial incentives for schools that didn’t already stock epinephrine autoinjector to start stocking them. Joe Manchin, the father of Mylan's CEO, was a senator at that time.
In 2013, the company acquired an Indian generic injectable drugs company, Agila Specialties Private, for $1.6 billion. In 2015 three plants acquired in that deal were issued warning letters by the FDA.
Attempted Perrigo acquisition
In April 2015, the company attempted a hostile takeover of Perrigo, offering to buy $26 billion in shares directly from shareholders. Too few shareholders agreed to sell their stock by the deadline set in November 2015 and the effort failed.
Attempted purchase by Teva
Two weeks after the company made its first offer for Perrigo, Teva Pharmaceutical offered to buy the company for $40 billion; the combined companies would have been the world's largest generic company and the 9th biggest drug company in the world. In July, Teva dropped its bid for Mylan and instead acquired Allergan's generic drug business for about the same price.
New COPD drug
In June 2015, the company agreed to work with Pulmatrix, a company with a proprietary inhaled drug delivery platform, to co-develop a product to treat for chronic obstructive pulmonary disease; the product was PUR0200, a generic drug in a Pulmatrix device.
In February 2016, the company announced it would acquire Meda AB for $9.9 billion. In May 2016, the company announced it would acquire Renaissance Acquisition Holdings dermatology division for up to $1 billion.
In December 2016, the State attorney generals of 20 states filed a civil complaint accusing the company of a coordinated scheme to artificially maintain high prices for a generic antibiotic and diabetes drug. The complaint alleged price collusion schemes between six pharmaceutical firms including informal gatherings, telephone calls, and text messages.
In October 2017, the company announced the launch of the first FDA-approved generic of Teva’s long-acting Copaxone. Approximately three months later, Credit Suisse analyst Vamil Divan cited IMS Health data which showed that the new generic accounted for 10% of the market.
In May 2018, the company announced a collaboration with West Virginia University to expose children across West Virginia to STEM educational initiatives.
Generic Advair approval
Merger with Pfizer's off-patent drug business and name change to Viatris
In November 2019, Mylan & Upjohn announced that the name of the new company would be Viatris. Mylan renamed itself Viatris, a name held by one of Mylan's subsidiaries. The company continued sales of Mylan's more than 7,500 products, including biosimilars, generics, brand and over-the-counter remedies, with brands including the Epi-Pen, Viagra, Lipitor and Celebrex.
On February 23, 1973, the company became a public company via an initial public offering (IPO), on the OTC market. In 1976, the stock moved to NASDAQ and in 1986, it moved to the New York Stock Exchange.
The following is an illustration of the company's major mergers and acquisitions and historical predecessors:
Mylan acquired the right to market and distribute the EpiPen line of epinephrine autoinjector devices from Merck KGaA as part of their 2007 deal; that right had formerly been held by Dey LP, a wholly owned subsidiary of Merck. According to Bloomberg the devices deliver about $1 worth of drug. At that time annual sales were around $200M. Bresch, the company's CEO, saw an opportunity to increase sales through marketing and advocacy, and the company launched a marketing campaign to increase awareness of the dangers of anaphylaxis for people with severe allergies that made the brand "EpiPen" as identified with its product as "Kleenex" is with facial tissue. The company also successfully lobbied the FDA to broaden the label to include risk of anaphylaxis and in parallel, successfully lobbied Congress to generate legislation making EpiPens available in schools and in public places like defibrillators are, and hired the same people that Medtronic had worked with on defibrillator legislation to do so. Mylan's efforts to gain market dominance were aided when Sanofi's competing product was recalled in November 2015 and further when Teva's generic competitor was rejected by the FDA in March 2016.
By the first half of 2015, Mylan had an 85% market share of such devices in the US and in that year sales reached around $1.5B and accounted for 40% of Mylan's profit. Those profits were also due in part to Mylan's continually raising the price of EpiPens starting in 2009; in 2009 the wholesale price of two EpiPens was about $100, by July 2013 the price was about $265, in May 2015 it was around $461, and in May 2016 the price rose again to around $609, around a 500% jump from the price in 2009.
Starting in 2014, according to a 2017 report in the New York Times, mid-level executives began questioning the rate at which the company had increased and was planning to continue to increase the price of the Epi-Pen, and raising concerns that the price increases were unethical; the Times reported that when these concerns were brought to Robert Coury, the chairman of the board, Coury "replied that he was untroubled. He raised both his middle fingers and explained, using colorful language, that anyone criticizing Mylan, including its employees, ought to go copulate with themselves. Critics in Congress and on Wall Street, he said, should do the same. And regulators at the Food and Drug Administration? They, too, deserved a round of anatomically challenging self-fulfillment." The Times reported that Bresch provided similarly dismissive responses. The reporter noted that "Those top leaders’ responses are a far cry from the message on Mylan’s website, which says that 'we challenge every member of every team to challenge the status quo,' and that 'we put people and patients first, trusting that profits will follow.'", and also noted that "The firm is a case study in the limits of what consumer and employee activism, as well as government oversight, can achieve." 
In the summer of 2016, as parents prepared to send their children back to school and went to pharmacies to get new EpiPens, people began to express outrage at the cost of the EpiPen and the company was widely and harshly criticized, including criticism from Martin Shkreli, "poster boy for grasping pharma greed," letters from two Senators and initiation of Congressional investigations. Mylan's pricing of the EpiPen was widely referred to as price gouging. The last price increase coincided with the company's airing of a new line of TV commercials that were described as "shocking" and "no holds barred", depicting an anaphylactic reaction from the point of view of the young woman having it at a party, and ending with the young woman seeing her swollen and hive-covered face in the mirror before she collapses. In response to criticism, the company increased financial assistance available for some patients to purchase EpiPens, a gesture that was called a "classic public relations move" by Harvard Medical School professor Aaron Kesselheim. The up to $300 saving cards can only be used by a small number of people who need the drug, and no one on Medicaid. They do nothing about the high price which is still being paid by insurers, who ultimately pass the cost onto consumers. The company further responded by releasing the first authorized generic version of the EpiPen in December 2016 at a more than 50% discount.
In September 2016, the New York State Attorney General began an investigation into the company's EpiPen4Schools program in New York to determine if the program's contracts violated antitrust law and the West Virginia State Attorney General opened an investigation into whether Mylan had given the state the correct discount under the Medicaid Drug Rebate Program and subpoenaed the company when it refused to provide the documentation the state requested.
In October 2016, the CEO of the company testified to Congress that Pfizer/King charged the company about $34.50 for one device. In September 2016, a Silicon Valley engineering consultancy performed a teardown analysis of the EpiPen and estimated the manufacturing and packaging costs at about $10 for a two-pack.
According to the Department of Health and Human Services' Office of Inspector General analysis, the U.S. government may have overpaid "as much as $1.27 billion between 2006 and 2016" to the company for the EpiPen emergency allergy treatment. This represents three times the proposed settlement of $465 million announced by the company in October 2016. In October 2016, the company announced a settlement with the US Department of Justice over rebates paid by the company to states under the Medicaid Drug Rebate Program. Questions had been raised by Congress and others about why EpiPen had been classified as a generic rather a proprietary product in the program since 1997; generic drugs have lower rebates (13%) than proprietary drugs (23%), and price hikes for generic drugs cannot be passed onto states, and a common form of pharmaceutical fraud involves misclassifying proprietary drugs as generic under the program. Under the agreement, the company agreed to pay a $465 million payment and to a sign a corporate integrity agreement requiring it to perform better in the future; the settlement also resolved cases brought by states related to the rebates. Simultaneously with the settlement, the company also announced it was being investigated by the Securities and Exchange Commission related to the drug rebate program. Republican Senator Chuck Grassley, chair of the Senate Judiciary Committee that launched the "probe of EpiPen pricing probe in 2016, released the analysis on May 30, 2017. On the same day, a group of Mylan "investment funds urged shareholders to vote against the re-election of the company's directors after it paid Chairman Robert Coury over $97 million last year."
The company manufactures rocuronium bromide, which is approved by the state of Alabama for use in executions by lethal injection. European manufacturers refuse to sell drugs which can be used for executions to the United States, except to distributors or users who sign legally binding agreements that the drug will not be used for executions down the delivery chain.
In September 2014, the London-based human rights organisation Reprieve told the company that it was the only FDA-approved manufacturer of rocuronium bromide without legal controls in place to prevent its use in executions, and there was "a very real risk that Mylan may soon become the go-to provider of execution drugs for states across the country". German asset manager DJE Kapital divested itself of $70 million in Mylan shares for that reason. The company said that its distribution was "legally compliant,"  and that their restrictions did "prohibit resale to correctional facilities for use in lethal injections." 
|Penicillin G tablets||Antibiotic||1966|
Upon closing of the Pfizer merger in November 2020, Michael Goettler became CEO, Robert J. Coury as Chairman, Sanjeev Narula AS CFO and Rajiv Malik will continue as President of the new company.
- "Mylan N.V. 2018 Annual Report (Form 10-K)". last10k.com. U.S. Securities and Exchange Commission. February 2019.
- Mylan NV 10-K for the Fiscal Year Ended December 31, 2015
- "Mylan buys part of drug maker". American City Business Journals. December 18, 2006.
- "Mylan Laboratories To Acquire Generics Business Of Merck KGaA For 4.9 Billion Euros". Medical News Today. May 26, 2007.
- "Pharmaceutical giants tracking Mylan's prosperity". The Pittsburgh Tribune-Review. August 13, 2008. Archived from the original on September 8, 2008.
- "Therapeutic Innovation". www.mylan.com. Retrieved August 8, 2018.
- Egan, Matt. "EpiPen maker faces revolt over exec's $98 million pay package". CNN Money.
- "Mylan's Morgantown Facility is Mammoth State of the Art". Retrieved June 11, 2018.
- "Mylan Pharmaceuticals ULC: Private Company Information - Bloomberg". www.bloomberg.com. Retrieved June 11, 2018.
- "Mylan Technologies Inc. Expands, Adds 160 New Jobs | BioSpace". BioSpace. Retrieved June 11, 2018.
- "Somerset Pharmaceuticals, Inc.: Private Company Information - Bloomberg". www.bloomberg.com. Retrieved June 11, 2018.
- "Brand Name Medicines - Mylan". dey.com.
- "About Us". mylan.com.
- "Dey Pharma to Change to Mylan". American City Business Journals. February 15, 2012.
- "Contatar | Mylan". www.mylan.com.br. Retrieved June 11, 2018.
- "Better health for a better world" (PDF). March 2016. Retrieved June 11, 2018.
- "Japan Pharmaceutical Manufacturers Association (JPMA)". www.jpma.or.jp. Retrieved June 11, 2018.
- "Contact | Mylan". www.mylan.com.au. Retrieved June 11, 2018.
- "Agila Specialties Private Limited: Private Company Information - Bloomberg". www.bloomberg.com. Retrieved June 11, 2018.
- "Mylan recalls Bangalore unit cancer drug". dna. June 16, 2015. Retrieved June 11, 2018.
- "About Us". mylan.com.
- "Generics Pharma Hellas E.P.E.: Private Company Information - Bloomberg". www.bloomberg.com. Retrieved June 11, 2018.
- "Mylan to create 500 jobs in €380m expansion". RTE.ie. April 18, 2012. Retrieved June 11, 2018.
- "Committee on Energy and Commerce" (PDF). Retrieved June 11, 2018.
- Dearment, Alaric (October 10, 2011). "Milan Puskar, co-founder of Mylan, dies". Drug Store News.
- "A Tale of Two Entrepreneurs". www.wvexecutive.com. Retrieved July 1, 2018.
- Seaman, John T.; Landry, John T. (April 10, 2012). Mylan: 50 Years of Unconventional Success: Making Quality Medicine Affordable and Accessible. UPNE. ISBN 9781611682700.
- "Mylan 50 years young and still making history". Mylan.
- Freudenheim, Milt (September 10, 1989). "Exposing the F.D.A.". The New York Times.
- "Mylan Laboratories". www.thepharmaletter.com.
- Lewis, Ralph A. (1992). "The Emerging Effects of the Drug Price Competition and Patent Term Restoration Act of 1984". Journal of Contemporary Health Law & Policy. 8 (1): 361–378. PMID 10118987.
- "COMPANY NEWS; SmithKline Loses Drug Exclusivity". The New York Times. Reuters. August 22, 1987.
- Boehm, Garth; Yao, Lixin; Han, Liang; Zheng, Qiang (September 2013). "Development of the generic drug industry in the US after the Hatch-Waxman Act of 1984". Acta Pharmaceutica Sinica B. 3 (5): 297–311. doi:10.1016/j.apsb.2013.07.004.
- John Seaman and John T. Landry. Mylan 50 Years of Unconventional Success. Mylan, in association with University Press of New England, 2011. ISBN 9781611682700. Page 50
- Strickland, Carol (October 15, 1989). "Bolar: A Drug Company Under Siege". The New York Times.
- Shaw, Donna (February 27, 1991). "U.s. Charges Bolar Pharmaceutical With Misrepresenting Its Products". Philadelphia Inquirer.
- Freudenheim, Milt (February 28, 1991). "Bolar Plans Guilty Plea On Generics". The New York Times.
- Pink Sheet October 22, 1984 Mylan's Maxzide is "Approvable" at FDA: Lederle To Market Brand Competition to Smithkline's No. 3-Ranked Dyazide; Final Approval Anticipated "Imminently"
- FDA Approval History NDA 019129: Maxzide Page accessed September 8, 2016
- Reid, Kenneth (November 17, 1987). "US Judge to Rule on Drug Marketing". The Journal of Commerce.
- Andrews, Edmund L. (July 31, 1989). "F.D.A. Inquiry on Generic Drugs Focuses on Changes in Ingredients". The New York Times.
- Cimons, Marlene (August 29, 1989). "FDA to Lift OK of Last Dyazide Generic Version". Los Angeles Times.
- "Bolar and Mylan Team to Purchase Somerset Labs". Pink Sheet. November 14, 1988.
- "Somerset Eldepryl June 5 Approval Clears Way For Mylan/Bolar Acquisition". Pink Sheet. June 12, 1989.
- Ku, Mannching Sherry (December 1, 2015). "Recent trends in specialty pharma business model". Journal of Food and Drug Analysis. 23 (4): 595–608. doi:10.1016/j.jfda.2015.04.008. PMID 28911475.
- "Mylan 1996 Form 10-K Annual Report".
- Labaton, Stephen (December 5, 1998). "A Drug Maker Is Said to Face A Suit on Prices". The New York Times.
- "Press release: FTC Reaches Record Financial Settlement To Settle Charges of Price-fixing in Generic Drug Market | Federal Trade Commission". FTC. November 29, 2000.
- Labaton, Stephen (July 13, 2000). "Generic-Drug Maker Agrees to Settlement In Price-Fixing Case". The New York Times.
- Creswell, Julie (March 21, 2005). "Icahn the Spoiler". [[Fortune (magazine}|Fortune]].
- Pollack, Andrew (November 20, 2004). "Icahn Offers $5.4 Billion for Mylan, Drug Maker". The New York Times.
- O'keefe, Eric (May 12, 2005). "Icahn Slate Wins Seats on Blockbuster Board". The New York Times.
- Lazo, Shirley A. "Survival Strategy". Barron's.
- "Icahn Drops Bid for Mylan". Los Angeles Times. Bloomberg News. July 29, 2005.
- "Mylan Signs US$736-mil. Takeover Deal for India's Matrix Laboratories". IHS. August 28, 2006.
- "Mylan's Acquisition of Matrix: Business Strategy Case Study". ICRM.
- Massey, Steve (May 13, 2007). "Mylan buys Merck generic drug unit for $6.6 billion". Pittsburgh Post-Gazette.
- "Press release: Mylan Completes Acquisition of Generics Business of Merck KGaA". Mylan. October 2, 2007.
- "Mylan completes acquisition of Merck's generic unit". PM Live. September 30, 2008.
- Cynthia Koons and Robert Langreth for Bloomberg Businessweek. September 23, 2015 How Marketing Turned the EpiPen Into a Billion-Dollar Business
- Johnson, Carolyn Y.; Ho, Catherine (August 25, 2016). "How Mylan, the EpiPen company, maneuvered to create a virtual monopoly". The Chicago Tribune.
- Adams, Russell (October 30, 2009). "Mylan Again Sues Pittsburgh Post-Gazette". The Wall Street Journal.
- Sabatini, Patricia; Boselovic, Len (July 26, 2009). "Mylan workers overrode drug quality controls Internal report detailed 'pervasive' practice of ignoring safety procedures". Pittsburgh Post-Gazette.
- Edwards, Jim (July 28, 2009). "It's Not Mylan's First Quality Control Beef With FDA". CBS News.
- "Mylan, Pittsburgh Post-Gazette settle lawsuits". CBS News. Associated Press. February 17, 2012.
- "Four Pharmaceutical Companies Pay $124 Million for Submission of False Claims to Medicaid" (Press release). US Department of Justice. October 19, 2009.
- "Mylan acquires rights to Pfizer's inhaler technology". drugstorenews.com. Archived from the original on May 9, 2015.
- Stanton, Dan (June 8, 2015). "GSK breathes freely as Mylan launches Seretide generic in UK". in-Pharma Technologist.
- Helfand, Carly (February 22, 2016). "Mylan joins the Advair-copycat queue, but approval could be a long slog". Questex.
- Swetlitz, Ike; Silverman, Ed (August 26, 2016). "Mylan may have violated antitrust law in its EpiPen sales to schools". PBS Newshour.
- O'Donnell, Jayne (September 21, 2016). "Family matters: EpiPens had high-level help getting into schools". USA Today.
- Novak, Matt (August 23, 2016). "How Congress, the FDA, and Sarah Jessica Parker Helped EpiPen Become a $1 Billion Business". Gizmodo.
- Thomas, Katie (February 27, 2013). "Mylan Buys Drug Maker of Generic Injectables". The New York Times.
- Palmer, Eric (August 18, 2015). "UPDATED: FDA castigates three Mylan sterile drug plants in warning letter". Questex.
- "Mylan Completes Acquisition Of Abbott's Non-U.S. Developed Markets Specialty And Branded Generics Business" (Press release). Business Wire. February 27, 2015.
- Tascarella, Patty (February 27, 2015). "Mylan inversion deal completed". American City Business Journals.
- "US drugmaker Mylan to acquire Famy Care for $750 Million". Times Internet. February 3, 2015.
- Nathan, Vidya L. (February 3, 2015). "Mylan buys female health businesses from Indian drugmaker". Reuters.
- Koons, Cynthia (November 13, 2015). "Mylan's Hostile Bid for Perrigo Fails". Bloomberg.
- Kareen Nair, Samantha (November 13, 2015). "Mylan fails in $26 billion takeover bid for Perrigo". Reuters.
- WIECZNER, JEN (November 13, 2015). "Why Mylan Just Lost The Largest Hostile Takeover Battle Ever". Fortune.
- Rockoff, Jonathan D.; Mattioli, Dana (April 22, 2015). "Teva Offers to Buy Mylan for $40 Billion". The Wall Street Journal.
- "Teva to Buy Allergan's Generic Drug Unit". Bloomberg News. July 27, 2015.
- Somayaji, Chitra (July 27, 2015). "Teva Snaps Up Allergan's Generics Arm, Dumping Mylan". Bloomberg News.
- "Mylan to Co-Develop Pulmatrix' COPD Candidate". Mary Ann Liebert. June 16, 2015.
- "Mylan to Acquire Meda for $9.9B". Mary Ann Liebert. February 11, 2016.
- "Mylan snaps up dermatology biz from investors in $1B deal". Questex.
- Thomas, Katie (December 15, 2016). "20 States Accuse Generic Drug Companies of Price Fixing". The New York Times.
- Helfand, Carly (January 4, 2018). "Look out, Teva: Mylan's Copaxone copy has already captured serious share". Questex.
- Hudock, Megan (May 14, 2018). "Mylan and WVU announce 10 year collaboration". WBOY-TV.
- "Mylan Expands Its Voluntary Nationwide Recall of Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide Tablets, USP, to all Lots Within Expiry Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in the Active Pharmaceutical Ingredient" (Press release). Food and Drug Administration. December 4, 2018.
- "FDA approves first generic Advair Diskus" (Press release). Food and Drug Administration. January 30, 2019.
- Ponnezhath, Maria (July 27, 2019). "Pfizer in talks to merge off-patent drugs business with Mylan: source". Reuters.
- "Investor Presentations – August 2020 - Path to Shareholder Value Creation VIATRIS TSR Execution Plan" (PDF). Champion For Global Health. Retrieved October 22, 2020.
- Sabatini, Patricia (November 12, 2019). "Viatris picked as new name for a merged Mylan/Upjohn". Pittsburgh Post-Gazette.
- Blankenship, Kyle (November 12, 2019). "Pfizer's Upjohn and Mylan will become Viatris. Wait, haven't we heard that name before?". Questex.
- Brozak, Steve (July 29, 2019). "What The Pfizer-Mylan Deal Means For Pharma". Forbes. Retrieved December 10, 2019.
- "Mylan's Merger with Pfizer's Off-Patent Drug Unit Will Create 'New Champion for Global Health'". BioSpace. Retrieved May 11, 2020.
- "Pfizer to spinoff, merge off-patent drugs unit with Mylan". Reuters. July 29, 2019. Retrieved May 11, 2020.
- "Mylan Upjohn Merger – Pfizer Shareholders to receive 0.12 Viatris Shares per Pfizer Share". Mr. Virk Media.
- "Mylan to buy Agila Specialties from India's Strides for $1.6 bln". Reuters. February 27, 2013.
- "Mylan to acquire Pfizer respiratory tech for $17.5M". Questex.
- Grogan, Kevin (July 15, 2010). "Mylan acquires Ireland's Bioniche Pharma". www.pharmatimes.com. Retrieved June 11, 2018.
- "US pharma major Mylan buys Matrix Labs". The Economic Times. August 29, 2006. Retrieved June 11, 2018.
- "Mylan Fleshing Out Deal for Penederm / Skin-drug firm to sell for $205 million". SFGate. Retrieved June 11, 2018.
- "Mylan Labs, Dow B. Hickam set plans for stock-swap merger". United Press International. June 27, 1991.
- "Mylan buys out Watson's interest in Somerset Pharmaceuticals". American City Business Journals. July 28, 2008.
- Parker-Pope, Tara; Peachman, Rachel Rabkin (August 22, 2016). "EpiPen Price Rise Sparks Concern for Allergy Sufferers". The New York Times.
- King Pharmaceuticals October 21, 2002. Press Release: King Pharmaceuticals to Acquire Meridian Medical Technologies
- Helfand, Carly (March 1, 2016). "FDA swats down Teva's EpiPen copy, putting Mylan in cruise control". Questex.
- Willingham, Emily (August 21, 2016). "Why Did Mylan Hike EpiPen Prices 400%? Because They Could". Forbes.
- Bartolotta, Devin (August 18, 2016). "Cost Jumps Nearly 500-Percent For Life-Saving EpiPens". CBS Baltimore. Retrieved August 19, 2016.
- Duhigg, Charles (June 4, 2017). "Outcry Over EpiPen Prices Hasn't Made Them Lower". The New York Times.
- Novak, Matt (June 5, 2017). "Drug Company Chairman to America: Go Fuck Yourself". Gizmodo.
- Mole, Beth (June 5, 2017). "Mylan chairman: Drug pricing critics ought to go copulate with themselves". Ars Technica.
- Loew, Derek (June 12, 2017). "Mylan Begins Harvesting the Crop It's Sown". Science.
- Goldberg, Kenny (February 18, 2016). "People With Food Allergies Say Life-Saving Drug Too Expensive". KPBS Public Media.
- Walker, Joseph; Winslow, Ron; Steele, Anne (August 30, 2016). "Mylan to Launch Cheaper Generic EpiPen Alternative". The Wall Street Journal.
- Court, Emma (August 18, 2016). "Mylan's EpiPen price increases are Valeant-like in size, Shkreli-like in approach". MarketWatch.
- Tuttle, Brad (August 22, 2016). "5 Signs That EpiPen Prices Are Completely Out of Control". Time.
- Hiltzik, Michael (August 23, 2016). "Another reason to hate Mylan, which jacked up the price of life-saving EpiPens: It's a tax dodger". Los Angeles Times.
- Matt Novak for Gizmodo. August 23, 2016 How Congress, the FDA, and Sarah Jessica Parker Helped EpiPen Become a $1 Billion Business
- Bulik, Beth Snyder (May 1, 2016). "No holds barred in Mylan's ultra-realistic peanut allergy campaign". Questex.
- "Mylan to provide EpiPen cost assistance as CEO is asked to testify on price hike". The Guardian. August 25, 2016.
- Carolyn Y. Johnson (August 25, 2016). "Why Mylan's 'savings card' won't make EpiPen cheaper for all patients". The Washington Post.
- Ramsey, Lydia (December 16, 2016). "The $300 generic EpiPen is here". Business Insider.
- Larson, Erik; Hopkins, Jared S. (September 6, 2016). "Mylan's EpiPen School Sales Trigger N.Y. Antitrust Probe". Bloomberg. Retrieved September 7, 2016.
- Feeley, Jef; Langreth, Robert (September 20, 2016). "Mylan Investigations Mount as West Virginia Opens Fraud Probe". Bloomberg News.
- Popken, Ben (September 30, 2016). "Upgraded EpiPens torn apart. Tech firm: "It's the same core device"". NBC News.
- Tracy, Seipel. "Silicon Valley engineers figure real cost to make lifesaving auto-injector two-pack". The Mercury News. Retrieved October 1, 2016.
- Thomas, Katie (October 7, 2016). "Mylan to Settle EpiPen Overpricing Case for $465 Million". The New York Times.
- Thomas, Katie (September 2, 2016). "Is EpiPen a Brand-Name or a Generic Drug? Mylan Casts It Both Ways". The New York Times.
- Mole, Beth (October 7, 2016). "For ripping off Medicaid, EpiPen maker Mylan pays Feds $465 million". Ars Technica. Retrieved October 8, 2016.
- Tracer, Zachary (October 7, 2016). "Mylan Agrees to $465 Million EpiPen Settlement With U.S." Bloomberg.com.
- Erman, Michael (May 31, 2017). "Mylan may have overcharged U.S. for EpiPen by $1.27 billion: HHS". Reuters. New York. Retrieved May 31, 2017.
- Owen Dyer (October 24, 2014). "Drug company is targeted for refusing to adopt ban on distribution of execution drug". BMJ. 2014 (349): g6452. doi:10.1136/bmj.g6452. PMID 25344344. S2CID 21513100.
- "Mylan Statement on its Policy Against the Use of Mylan Products in Capital Punishment". Mylan. Retrieved June 25, 2018.
- "Milan Puskar, co-founder of Mylan, dies - Drug Store News". Drug Store News. October 10, 2011. Retrieved July 17, 2018.
- "Drugs@FDA: FDA Approved Drug Products". www.accessdata.fda.gov. Retrieved July 17, 2018.
- "Drugs@FDA: FDA Approved Drug Products". www.accessdata.fda.gov. Retrieved July 17, 2018.
- "FDA approves generic forms of ciprofloxacin". CIDRAP. Retrieved July 17, 2018.
- "MYLAN's MAXZIDE IS "APPROVABLE" AT FDA: LEDERLE TO MARKET BRAND COMPETITION TO SMITHKLINE's No. 3-RANKED DYAZIDE; FINAL APPROVAL ANTICIPATED "IMMINENTLY"". Pink Sheet. October 22, 1984. Retrieved July 17, 2018.
- "SOMERSET ELDEPRYL JUNE 5 APPROVAL CLEARS WAY FOR MYLAN/BOLAR ACQUISITION". Pink Sheet. June 12, 1989. Retrieved July 17, 2018.
- Kusjanto, Mantik. "Merck KGaA sells generics unit to Mylan for $6.6 bln". U.S. Retrieved July 17, 2018.
- "Why the CEO Behind the EpiPen Controversy Is on Fortune's Most Powerful Women List". Fortune.
- Staton, Tracy (June 15, 2017). "As rebel Mylan investors win more backing, CEO Bresch champions her board". Questex.
- GATLIN, ALLISON (September 22, 2017). "Generic Drug Makers Face Pricing Issues Unlike Other Pharmaceutical Companies". Investor's Business Daily.
- "Investor Presentation Aug 2020 - Page 5 -Introducing VIATRIS' New Executive Management Team" (PDF). championforglobalhealth.com. Retrieved October 22, 2020.