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ondansetron hydrochloride

NDC 83270-161 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerOnesource Specialty Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078257
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsONDANSETRON HYDROCHLORIDE (2 mg/mL)
Marketing started20230930
Package count1

External sources

Source: openFDA. Public-domain (CC0).