United States · FDA National Drug Code directory
Ciclopirox
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 68788-6797_d8e8b3d5-07e7-4b46-994a-b642ecf947ce
- Product NDC
- 68788-6797
- Form
- SOLUTION
- Composition / generic term
- Ciclopirox
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161103
- Source listing expiry
- 20271231
Source-listed ingredients
- CICLOPIROX — 80 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68788-6797-6) / 6.6 mL in 1 BOTTLE, WITH APPLICATOR · 68788-6797-6
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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