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Lupin Launches Sugammadex Injection in US Following FDA Approval

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Lupin said Thursday it has launched Sugammadex Injection in the US following approval from the US Food and Drug Administration.

The firm said the drug, a bioequivalent to Merck's (MRK) Bridion Injection, is indicated for the reversal of neuromuscular blockade induced by rocuronium bromide and vecuronium bromide in adults and pediatric patients aged 2 years and older undergoing surgery.

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