# CIPRO HC

NDC: 66758-087
Generic name: ciprofloxacin hydrochloride and hydrocortisone
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUSPENSION/ DROPS
Routes: AURICULAR (OTIC)
Marketing started: 19990315

FDA application: NDA020805

## Active ingredients

- CIPROFLOXACIN HYDROCHLORIDE: 2 mg/mL
- HYDROCORTISONE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"66758-087"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66758-087
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b26594a3-2adf-4954-8be0-5bd6f8de9671