United States · FDA National Drug Code directory
Acitretin
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
- 0093-1138_11579624-a4a1-4db1-bf72-9fbedbce3225
- Product NDC
- 0093-1138
- Form
- CAPSULE
- Composition / generic term
- Acitretin
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130719
- Source listing expiry
- 20261231
Source-listed ingredients
- ACITRETIN — 17.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (0093-1138-56) · 0093-1138-56
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 →