U.S. FDA approval and launch of Sugammadex Injection
LUPIN · price
▲ positive · ▼ negative · ● neutral filings · teal = economic event · numbered = multiple that day (click to pick). Times IST.
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Lupin received U.S. FDA approval for its Abbreviated New Drug Application and launched Sugammadex Injection (200 mg/2 mL and 500 mg/5 mL single-dose vials) in the United States. It is the bioequivalent of Merck's Bridion Injection and is used to reverse neuromuscular blockade in adults and pediatric patients aged 2 and older undergoing surgery.
Positive — new generic product launch in the key U.S. market, expected to add to U.S. revenues and strengthen Lupin's complex generics portfolio.