# ciprofloxacin

NDC: 63187-990
Generic name: ciprofloxacin
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20040910

FDA application: ANDA076639

## Active ingredients

- CIPROFLOXACIN HYDROCHLORIDE: 750 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-990"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-990
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4af3894a-8945-4b2d-bdf6-a83bbd415b89