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Ondansetron

NDC 0143-9890 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerWest-Ward Pharmaceuticals Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA076781
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsONDANSETRON HYDROCHLORIDE (2 mg/mL)
Marketing started20061226
Package count2

External sources

Source: openFDA. Public-domain (CC0).