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Zoledronic acid

NDC 68001-437 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic namezoledronic acid
Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA205279
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsZOLEDRONIC ACID (4 mg/5mL)
Marketing started20200629
Package count1

External sources

Source: openFDA. Public-domain (CC0).