The company is releasing the medication in 200 mg/2 mL and 500 mg/5 mL single-dose vials. This launch expands Lupin’s footprint in the competitive U.S. generic space, where the company maintains a broad portfolio spanning respiratory, cardiovascular, and central nervous system therapies. By providing a bioequivalent option to the established Bridion brand, Lupin aims to capture a share of the clinical market for patients aged two years and older.
In section Releases
Lupin Launches Sugammadex Generic in US Market
Mumbai-based pharmaceutical giant Lupin has officially entered the U.S. market with its Sugammadex Injection, securing FDA approval for the generic version of Merck’s Bridion. The rollout targets both adult and pediatric surgical patients, offering a bioequivalent alternative for the reversal of neuromuscular blockade induced by rocuronium or vecuronium bromide.
Lupin operates 15 manufacturing sites and seven research centers worldwide, supporting its distribution network across more than 100 countries. This latest regulatory clearance underscores the company's focus on complex generics and biotechnology, further diversifying its presence in the American healthcare sector.
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