FDA NDC Directory · JSON-LD · Markdown

ONDANSETRON

NDC 61919-565 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA078539
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/1)
Marketing started20190822
Package count2

External sources

Source: openFDA. Public-domain (CC0).