# Ciprofloxacin

NDC: 70934-965
Generic name: Ciprofloxacin Hydrochloride
Labeler / Manufacturer: Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220502
Marketing ended: 20260831
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:"70934-965"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70934-965
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de0b9579-fb85-e1ce-e053-2a95a90aeecb