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ONDANSETRON

NDC 51662-1469 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA077548
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsONDANSETRON HYDROCHLORIDE (2 mg/mL)
Marketing started20191214
Package count1

External sources

Source: openFDA. Public-domain (CC0).