# Ciprofloxacin

NDC: 71205-636
Generic name: Ciprofloxacin Hydrochloride
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20070426

FDA application: ANDA077859

## Active ingredients

- CIPROFLOXACIN HYDROCHLORIDE: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-636"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-636
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9ee1f252-a64e-4b72-a6f7-60298e827222