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VECURONIUM BROMIDE

NDC 55150-235 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerEugia US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206670
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVECURONIUM BROMIDE (10 mg/1)
Marketing started20181220
Package count1

External sources

Source: openFDA. Public-domain (CC0).