# ciprofloxacin

NDC: 85293-003
Generic name: ciprofloxacin
Labeler / Manufacturer: Umasuto, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250305

FDA application: ANDA076639

## Active ingredients

- CIPROFLOXACIN HYDROCHLORIDE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85293-003"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85293-003
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0c355077-7361-41d0-9e82-eb31beaf5daa