FDA NDC Directory · JSON-LD · Markdown

ONDANSETRON

NDC 60505-4939 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA203711
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsONDANSETRON HYDROCHLORIDE (2 mg/mL)
Marketing started20260929
Package count1

External sources

Source: openFDA. Public-domain (CC0).