FDA NDC Directory · JSON-LD · Markdown

Ondansetron

NDC 16714-671 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameOndansetron Hydrochloride
Labeler / ManufacturerNorthStar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078776
Dosage form / routeSOLUTION · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/5mL)
Marketing started20071128
Package count1

External sources

Source: openFDA. Public-domain (CC0).