Beclometasone Dipropionate

SAN FRANCISCO, May 1, 2026 /PRNewswire/ -- Legal Notice Did You Purchase, Pay for, or Provide Reimbursement for QVAR® and/or QVAR RediHaler® Inhalers? You Could Get Money from a Settlement. There is a Settlement in a class action lawsuit with Teva Pharmaceutical Industries Ltd.; Teva Pharmaceuticals USA, Inc.; Teva Branded Pharmaceutical Products R&D, Inc.; and Norton (Waterford) Ltd. (collectively, "Teva"). The lawsuit claims that Teva unlawfully kept generic versions of QVAR® and QVAR RediHaler® off the market, so consumers and third-party payors paid more for QVAR® and QVAR RediHaler® inhalers than they should have. Teva denies it did anything wrong. No one is claiming that QVAR® or QVAR RediHaler® Products are unsafe. Who is included in the Settlement? You may be included in the Settlement if you are a person or entity that, for consumption by yourself, your families, or your members, insureds, or beneficiaries, purchased, paid, and/or provided reimbursement for some or all of the purchase price of QVAR® and/or QVAR RediHaler® inhalers, from January 1, 2015, through July 31, 2025, other than for resale, in the following states and territories: Alaska, Arkansas, Arizona, California, Connecticut, Delaware, D.C., Florida, Hawaii, Illinois, Indiana, Iowa, Kansas, Maine, Massachusetts, Maryland, Michigan, Minnesota, Mississippi, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Rhode Island, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, West Virginia, Wisconsin, and Wyoming. A more detailed notice, including the full class definition and who is not included, is available at . What does the Settlement provide? Teva will pay $35 million into a Settlement Fund that will pay (1) money to eligible Class Members; (2) notice and administration costs; (3) service awards to the class representatives who brought the lawsuit; and (4) attorneys' fees, costs, and expenses. Teva will also remove/delist certain patents from the Food and Drug Administration's Orange Book, removing certain barriers to bringing generic versions of QVAR® to market. How can I get a payment? You must submit a valid Claim Form to apply for payment from the Settlement Fund. The amount of your payment will depend on the amount of QVAR® and QVAR RediHaler® products you purchased, the number of valid claims filed, and the amount of purchases represented by those valid claims. Claim Forms, and information on how to submit them, are available at . Claim Forms must be postmarked (if mailed) or received (if submitted online) on or before July 31, 2026 . What are my rights? Even if you do nothing, you will be bound by the Court's decisions. If you want to keep your right to sue Teva yourself, you must exclude yourself by June 15, 2026. If you do not exclude yourself, you may object to the Settlement by June 15, 2026. Detailed instructions about how to act on these rights are available at . The Court will hold a hearing on August 5, 2026 to consider whether to approve the Settlement, a request for attorneys' fees of up to 33% of the Settlement Fund, reimbursement of litigation costs and expenses up to $890,000, payment of reasonable notice and claims administration costs, and service awards of $25,000 to each of the four class representatives. You or your own lawyer may appear and speak at the hearing at your own expense. The Court may change these deadlines or the hearing date and time. Check the website below for updates. Please do not call the Court or the Clerk of the Court for information about the Settlement. For more information: 1-866-588-8524 SOURCE Berman Tabacco, Sperling Kenny Nachwalter, LLC and Hilliard Shadowen LLP 21% more press release views with Request a Demo

Launch of albuterol sulfate inhalation aerosol and beclomethasone dipropionate HFA inhalation aerosol BRIDGEWATER, N.J., April 14, 2026 (GLOBE NEWSWIRE) -- Amneal Pharmaceuticals, Inc. (“Amneal” or the “Company”) (Nasdaq: AMRX) today announced the U.S. launch of albuterol sulfate inhalation aerosol and beclomethasone dipropionate HFA inhalation aerosol, two widely prescribed respiratory products that were approved by the Food and Drug Administration (FDA) in 2025. These are the Company’s first two metered-dose inhalation (MDI) product launches in the U.S., marking Amneal’s entry into the complex inhalation category. Albuterol sulfate inhalation aerosol (90 mcg per actuation) is a generic equivalent of PROAIR ® HFA. Beclomethasone dipropionate HFA inhalation aerosol (40 mcg and 80 mcg per actuation) is a generic equivalent of the original QVAR ® Inhalation Aerosol, 40 mcg and 80 mcg. Both products utilize the hand-breath actuator device in which the cannister is depressed by the patient before inhaling. This option was previously discontinued for QVAR ® , creating a potential gap in patient choice. “The launch of these two important inhalation products marks a significant milestone for Amneal and underscores the continued expansion of our respiratory platform,” said Dr. Srinivas Kone, Senior Vice President and Chief Scientific Officer – Affordable Medicines. “Manufactured at our dedicated inhalation facility in Ireland, these complex products reflect our ability to develop and scale difficult-to-make formulations that address meaningful gaps in patient access. With multiple additional inhalation products in active development, we are building a durable and differentiated presence in this attractive category.” Product Information Albuterol Sulfate Inhalation Aerosol is indicated for the treatment or prevention of bronchospasm in patients 4 years of age and older with reversible obstructive airway disease, and for the prevention of exercise-induced bronchospasm in patients 4 years of age and older. The most common adverse reactions reported with the use of albuterol sulfate inhalation aerosol (≥3.0% and greater than placebo) include headache, tachycardia, pain, dizziness, pharyngitis, and rhinitis. For full prescribing information, see package insert here . Beclomethasone dipropionate HFA inhalation aerosol is a corticosteroid indicated for the maintenance treatment of asthma as prophylactic therapy in patients 5 years of age and older. It is not indicated for the relief of acute bronchospasm. The most common adverse reactions reported with the use of beclomethasone dipropionate HFA inhalation aerosol include headache, pharyngitis, upper respiratory tract infection, rhinitis, increased asthma symptoms, and sinusitis. For full prescribing information, please refer to the package insert here . According to IQVIA ® U.S. annual sales data, for the 12 months ended February 2026, albuterol sulfate inhalation aerosol had sales of approximately $1.5 billion, and beclomethasone dipropionate HFA inhalation aerosol had sales of approximately $321 million. All trademarks are property of their respective owners. About Amneal Amneal Pharmaceuticals, Inc. (Nasdaq: AMRX), headquartered in Bridgewater, New Jersey, is a diversified, global biopharmaceutical leader focused on expanding access to affordable and innovative medicines. Founded in 2002 by brothers and co-CEOs Chirag and Chintu Patel, Amneal was built on the belief that innovation only matters if it’s accessible. Today, Amneal has a diverse and growing portfolio of approximately 300 complex generic, specialty and biosimilar medicines, delivering over 160 million prescriptions each year, primarily in the United States. Our Affordable Medicines segment spans retail generics, injectables, and biosimilars. Our Specialty segment provides branded treatments in neurology, including Parkinson’s disease and migraine, and endocrinology. Our AvKARE segment distributes pharmaceuticals and medical products to U.S. federal, retail, and institutional customers. For more, please visit and follow us on LinkedIn . Cautionary Statement on Forward-Looking Statements Certain statements contained herein, regarding matters that are not historical facts, may be forward-looking statements (as defined in the U.S. Private Securities Litigation Reform Act of 1995). Such forward-looking statements include statements regarding management’s intentions, plans, beliefs, expectations, financial results, or forecasts for the future, including among other things: discussions of future operations; expected or estimated operating results and financial performance; and statements regarding our positioning, including our ability to drive sustainable long-term growth, and other non-historical statements. Words such as “plans,” “expects,” “will,” “anticipates,” “estimates,” and similar words, or the negatives thereof, are intended to identify estimates and forward-looking statements. The forward-looking statements contained herein are also subject generally to other risks and uncertainties that are described from time to time in the Company’s filings with the Securities and Exchange Commission, including under Item 1A, “Risk Factors” in the Company’s most recent Annual Report on Form 10-K and in its subsequent reports on Forms 10-Q and 8-K. Forward-looking statements included herein speak only as of the date hereof and we undertake no obligation to revise or update such statements to reflect the occurrence of events or circumstances after the date hereof. Investor Contact Anthony DiMeo VP, Investor Relations anthony.dimeo@amneal.com Media Contact Brandon Skop Sr. Director, Corporate Communications brandon.skop@amneal.com