Lupin launches Sugammadex Injection in U.S. market
Mumbai, July 31 -- Lupin announced that following approval from the United States Food and Drug Administration (U.S. FDA) for its Abbreviated New Drug Application, the company launched Sugammadex Injection, 200 mg/2 mL (100 mg/mL) and 500 mg/5 mL (100 mg/mL) Single-Dose Vial in the United States.
Published by HT Digital Content Services with permission from Capital Market....
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