Acitretin
- Product NDC
- 46708-741
- 11-digit product format
- 467080741
- Labeler code
- 46708
- Product ID
- 46708-741_77011f2b-a2e7-4a43-9ff3-29d73f322319
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acitretin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Alembic Pharmaceuticals Limited
- Application
- ANDA217774
- Marketing category
- ANDA
- Marketing start
- 2024-08-08
- Substance
- ACITRETIN
- Active strength
- 10 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 |
|---|
| 46708-741-30 | 46708074130 | 30 CAPSULE in 1 BOTTLE (46708-741-30) | 30 capsule | 2024-08-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Acitretin Capsules, USP | Alembic Pharmaceuticals Limited | 2024-08-09 | Human Prescription Drug Label | 1 |