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Zoledronic Acid

NDC 43598-233 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerDr. Reddy's Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091186
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsZOLEDRONIC ACID (4 mg/5mL)
Marketing started20230821
Package count1

External sources

Source: openFDA. Public-domain (CC0).