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Ondansetron

NDC 72572-520 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerCivica, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077541
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsONDANSETRON HYDROCHLORIDE (2 mg/mL)
Marketing started20191118
Package count1

External sources

Source: openFDA. Public-domain (CC0).