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Sugammadex

NDC 70710-1651 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214290
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSUGAMMADEX SODIUM (500 mg/5mL)
Marketing started20260702
Package count1

External sources

Source: openFDA. Public-domain (CC0).