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ONDANSETRON

NDC 51662-1539 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA076183
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/1)
Marketing started20211006
Package count1

External sources

Source: openFDA. Public-domain (CC0).