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
- 21922-053_c81092f6-fe1e-4f70-8699-69c4cdce214f
- Product NDC
- 21922-053
- Form
- SOLUTION
- Composition / generic term
- ciclopirox
- Labeler
- Encube Ethicals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231109
- Source listing expiry
- 20261231
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 (21922-053-51) / 6.6 mL in 1 BOTTLE, WITH APPLICATOR · 21922-053-51
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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