United States · FDA National Drug Code directory
Tretinoin
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
- 21922-079_916137d0-edab-466c-8ec9-ffbe7b6cf162
- Product NDC
- 21922-079
- Form
- CREAM
- Composition / generic term
- Tretinoin
- Labeler
- Encube Ethicals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250711
- Source listing expiry
- 20271231
Source-listed ingredients
- TRETINOIN — .25 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (21922-079-06) / 45 g in 1 TUBE · 21922-079-06
- 1 TUBE in 1 CARTON (21922-079-25) / 20 g in 1 TUBE · 21922-079-25
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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