# CICLOPIROX

NDC: 68788-8755
Generic name: ciclopirox
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: TOPICAL
Marketing started: 20241014

FDA application: ANDA077687

## Active ingredients

- CICLOPIROX: 80 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8755"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8755
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eb7b7163-2ee7-447a-b585-7a240070f84b