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Zoledronic acid

NDC 23155-170 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201783
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsZOLEDRONIC ACID (4 mg/5mL)
Marketing started20230831
Package count1

External sources

Source: openFDA. Public-domain (CC0).