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Ondansetron Hydrochloride

NDC 0054-0064 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076960
Dosage form / routeSOLUTION · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/5mL)
Marketing started20061226
Package count1

External sources

Source: openFDA. Public-domain (CC0).