# CIPRO HC

NDC: 50090-7631
Generic name: ciprofloxacin hydrochloride and hydrocortisone
Labeler / Manufacturer: A-S Medication Solutions
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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-7631"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-7631
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d2c40b07-dc39-46c6-8ea1-b288589a46d1