# Zoledronic Acid

NDC: 71288-806
Generic name: Zoledronic Acid
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20230605

FDA application: ANDA213371

## Active ingredients

- ZOLEDRONIC ACID: 5 mg/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-806"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-806
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8aac81ae-f92c-4f0b-b480-44badf72b5f5