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Ondansetron

NDC 51672-4091 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameondansetron hydrochloride
Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077009
Dosage form / routeSOLUTION · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/5mL)
Marketing started20071130
Package count1

External sources

Source: openFDA. Public-domain (CC0).