# ciprofloxacin

NDC: 80425-0499
Generic name: Ciprofloxacin
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20250320

FDA application: ANDA077568

## Active ingredients

- CIPROFLOXACIN HYDROCHLORIDE: 3 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0499"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0499
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=30cb2b42-aa4b-8cec-e063-6394a90aa615