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ondansetron hydrochloride

NDC 83980-018 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerIpca Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203761
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (8 mg/1)
Marketing started20260814
Package count3

External sources

Source: openFDA. Public-domain (CC0).