# Zoledronic Acid

NDC: 55111-688
Generic name: Zoledronic Acid
Labeler / Manufacturer: Dr.Reddy's Laboratories Ltd
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20130403

FDA application: ANDA091363

## 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:"55111-688"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-688
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f94a5c9e-74bc-d09e-cd65-394b2a5de2ad
