FDA NDC Directory · JSON-LD · Markdown

Ondansetron

NDC 71335-3073 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA090469
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsONDANSETRON (8 mg/1)
Marketing started20100412
Package count8

External sources

Source: openFDA. Public-domain (CC0).