FDA NDC Directory · JSON-LD · Markdown

Ondansetron

NDC 0121-4882 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryAbbreviated NDA (generic) · App ANDA078127
Dosage form / routeSOLUTION · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (4 mg/5mL)
Marketing started20260609
Package count1

External sources

Source: openFDA. Public-domain (CC0).