FDA NDC Directory · JSON-LD · Markdown

Granisetron

NDC 63323-318 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameGRANISETRON HYDROCHLORIDE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078096
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsGRANISETRON HYDROCHLORIDE (1 mg/mL)
Marketing started20091120
Package count1

External sources

Source: openFDA. Public-domain (CC0).