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Zoledronic Acid

NDC 68083-142 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic namezoledronic Acid
Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA205749
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsZOLEDRONIC ACID (4 mg/100mL)
Marketing started20180705
Package count1

External sources

Source: openFDA. Public-domain (CC0).