FDA NDC Directory · JSON-LD · Markdown

Zoledronic Acid

NDC 71288-806 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213371
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsZOLEDRONIC ACID (5 mg/100mL)
Marketing started20230605
Package count1

External sources

Source: openFDA. Public-domain (CC0).