FDA NDC Directory · JSON-LD · Markdown

ONDANSETRON

NDC 63187-236 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077851
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/1)
Marketing started20070625
Package count3

External sources

Source: openFDA. Public-domain (CC0).