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Ondansetron

NDC 0409-2271 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameONDANSETRON
Labeler / ManufacturerHospira, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077548
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsONDANSETRON HYDROCHLORIDE (2 mg/mL)
Marketing started20251201
Package count1

External sources

Source: openFDA. Public-domain (CC0).