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
- 46708-807_f46af408-0e68-4a78-8928-fc655c54d0c4
- Product NDC
- 46708-807
- Form
- CREAM
- Composition / generic term
- Tretinoin
- Labeler
- Alembic Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250425
- Source listing expiry
- 20261231
Source-listed ingredients
- TRETINOIN — 1 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (46708-807-20) / 20 g in 1 TUBE · 46708-807-20
- 1 TUBE in 1 CARTON (46708-807-45) / 45 g in 1 TUBE · 46708-807-45
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 →