# Zoledronic acid

NDC: 23155-170
Generic name: Zoledronic acid
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20230831

FDA application: ANDA201783

## 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:"23155-170"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-170
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=00a5bd5a-e5ee-4bad-b510-a4d4485485c8