# Zoledronic Acid

NDC: 55111-685
Generic name: Zoledronic Acid
Labeler / Manufacturer: Dr. Reddy's Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20130304

FDA application: ANDA091186

## Active ingredients

- ZOLEDRONIC ACID: 4 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55111-685"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-685
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1738a682-5903-b675-3a7a-61d299a6f248