# Ciprofloxacin

NDC: 68071-3737
Generic name: Ciprofolxacin
Labeler / Manufacturer: NuCare Pharmaceutical, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20231001

FDA application: ANDA208921

## 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:"68071-3737"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3737
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=288ea7b2-ecf2-e8e0-e063-6294a90a306a