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ondansetron

NDC 55154-7879 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameondansetron hydrochloride
Labeler / ManufacturerCardinal Health 107, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076183
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (8 mg/1)
Marketing started20061226
Package count1

External sources

Source: openFDA. Public-domain (CC0).