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ONDANSETRON

NDC 23155-548 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079224
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsONDANSETRON HYDROCHLORIDE (2 mg/mL)
Marketing started20151109
Package count2

External sources

Source: openFDA. Public-domain (CC0).