ACITRETIN
- Product NDC
- 72162-2223
- 11-digit product format
- 721622223
- Labeler code
- 72162
- Product ID
- 72162-2223_5f10fb7f-f38a-42a0-9092-f67d7ea1e7cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ACITRETIN
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204633
- Marketing category
- ANDA
- Marketing start
- 2015-09-16
- Substance
- ACITRETIN
- Active strength
- 25 mg/1
- Pharmacologic classes
- Retinoid [EPC], Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| LCH760E9T7 | ACITRETIN | 55079-83-9 | ACITRETIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2223-3 | 72162222303 | 30 CAPSULE in 1 BOTTLE (72162-2223-3) | 30 capsule | 2024-01-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ® Tablets | Bryant Ranch Prepack | 2024-01-26 | HUMAN PRESCRIPTION DRUG LABEL | 100 |