FDA NDC Directory · JSON-LD · Markdown

PALONOSETRON

NDC 63323-673 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namePalonosetron
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206802
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsPALONOSETRON HYDROCHLORIDE (.25 mg/5mL)
Marketing started20180919
Package count1

External sources

Source: openFDA. Public-domain (CC0).