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sugammadex

NDC 76045-219 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA219448
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSUGAMMADEX SODIUM (100 mg/mL)
Marketing started20260728
Package count2

External sources

Source: openFDA. Public-domain (CC0).