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Rocuronium Bromide

NDC 71839-142 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namerocuronium bromide
Labeler / ManufacturerBE Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216234
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsROCURONIUM BROMIDE (10 mg/mL)
Marketing started20230712
Package count1

External sources

Source: openFDA. Public-domain (CC0).