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
- 21922-042_8cc4690a-be86-4f4a-8bd1-ff9f5d5d5747
- Product NDC
- 21922-042
- Form
- GEL
- Composition / generic term
- Tretinoin
- Labeler
- Encube Ethicals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260416
- Source listing expiry
- 20271231
Source-listed ingredients
- TRETINOIN — .6 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PUMP in 1 CARTON (21922-042-40) / 50 g in 1 BOTTLE, PUMP · 21922-042-40
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →