FDA NDC Directory · JSON-LD · Markdown

ONDANSETRON

NDC 51662-1245 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA077541
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsONDANSETRON HYDROCHLORIDE (2 mg/mL)
Marketing started20180923
Package count2

External sources

Source: openFDA. Public-domain (CC0).