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Granisetron Hydrochloride

NDC 67457-861 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerMylan Institutional LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091136
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsGRANISETRON HYDROCHLORIDE (.1 mg/mL)
Marketing started20180321
Package count0

External sources

Source: openFDA. Public-domain (CC0).