# Ciprofloxacin

NDC: 71610-081
Generic name: Ciprofloxacin
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20091010

FDA application: ANDA076126

## 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:"71610-081"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-081
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c7bc0d20-526c-48ea-b23a-cea9eb7080ff