FDA NDC Directory · JSON-LD · Markdown

Palonosetron

NDC 68001-355 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA201533
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsPALONOSETRON HYDROCHLORIDE (.05 mg/mL)
Marketing started20180530
Package count1

External sources

Source: openFDA. Public-domain (CC0).