# Ciprofloxacin

NDC: 60687-860
Generic name: Ciprofloxacin Hydrochloride
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240930
Marketing ended: 20270831
FDA application: ANDA077859

## 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:"60687-860"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-860
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0fac4466-fbe5-49d2-96e3-e3ac2739bd5b