sodium oxybate oral solution

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Amneal Receives U.S. FDA Approval of Sodium Oxybate Oral Solution
Globenewswireยท 2025-09-11 12:00
Core Insights - Amneal Pharmaceuticals has received FDA approval for its sodium oxybate oral solution 500 mg/mL, expanding its Affordable Medicines portfolio and providing a more affordable alternative for narcolepsy treatment [1][3]. Company Overview - Amneal Pharmaceuticals, Inc. is a global biopharmaceutical company headquartered in Bridgewater, NJ, with a diverse portfolio of over 280 pharmaceuticals, primarily in the U.S. [4]. - The company operates in various segments, including Affordable Medicines, Specialty, and AvKARE, focusing on complex product categories and therapeutic areas [4]. Product Details - Sodium oxybate is a central nervous system depressant used to treat cataplexy and excessive daytime sleepiness in patients aged 7 and older with narcolepsy [2]. - The approval of sodium oxybate oral solution addresses a critical therapy area for approximately 150,000 individuals in the U.S. living with narcolepsy [3]. Market Impact - The introduction of sodium oxybate by Amneal is significant as it provides patients, providers, and payers with a more affordable option in a market historically dominated by a single manufacturer [3].