# Zoledronic Acid

NDC: 55150-266
Generic name: Zoledronic Acid
Labeler / Manufacturer: AuroMedics Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20160926

FDA application: ANDA207751

## 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:"55150-266"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55150-266
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ac7ff1eb-6e73-4cc8-9114-c5a4483ad4c3
