FDA NDC Directory · JSON-LD · Markdown

Ondansetron Hydrochloride

NDC 55700-627 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerQuality Care Products LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078539
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (8 mg/1)
Marketing started20180518
Marketing ended20280131
Package count3

External sources

Source: openFDA. Public-domain (CC0).