# ciprofloxacin

NDC: 42708-192
Generic name: ciprofloxacin
Labeler / Manufacturer: QPharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20040910

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:"42708-192"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42708-192
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4149d980-a6cd-c06d-e063-6394a90a47a1