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Ondansetron Hydrochloride

NDC 67046-1242 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078539
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (8 mg/1)
Marketing started20260616
Package count1

External sources

Source: openFDA. Public-domain (CC0).