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Ondansetron

NDC 17856-0672 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameOndansetron Hydrochloride
Labeler / ManufacturerAtlantic Biologics Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA078776
Dosage form / routeSOLUTION · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/5mL)
Marketing started20071128
Package count4

External sources

Source: openFDA. Public-domain (CC0).