FDA NDC Directory · JSON-LD · Markdown

Zoledronic Acid

NDC 55150-266 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerAuroMedics Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207751
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsZOLEDRONIC ACID (4 mg/5mL)
Marketing started20160926
Package count1

External sources

Source: openFDA. Public-domain (CC0).