# Zoledronic Acid

NDC: 43598-233
Generic name: Zoledronic Acid
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20230821

FDA application: ANDA091186

## Active ingredients

- ZOLEDRONIC ACID: 4 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-233"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-233
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=72623e70-9db3-f1b8-de7d-c1a61d71fb01