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Lupin Receives Tentative FDA Approval for Sugammadex Injection

Lupin Limited logoLupin Limited
Sig2.91Sen+5.03Env0.00Soc+1.41Gov+1.13

Lupin received tentative U.S. FDA approval for its sugammadex injection, including 200 mg/2 mL and 500 mg/5 mL strengths, for reversing neuromuscular blockade from rocuronium bromide and vecuronium bromide in surgical patients aged 2 and older. Separately, its Philippine unit Multicare Pharmaceuticals Philippines completed a share buyback of 2,813,811 shares using retained earnings, reported under SEBI disclosure rules.

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