ACITRETIN
- Product NDC
- 72162-2224
- 11-digit product format
- 721622224
- Labeler code
- 72162
- Product ID
- 72162-2224_78bc5a42-251a-471b-a944-9219c7df1353
- 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
- 17.5 mg/1
- Pharmacologic classes
- Retinoid [EPC], Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ACITRETIN
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACITRETIN | 17.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | LCH760E9T7 |
| Rxcui | 894859 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2224-3 | ACITRETIN | 30 in 1 BOTTLE | CAPSULE | 30 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2224 | ACITRETIN CAPSULE [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240127_a5be620f-d721-40c1-a062-d21c70bfcbed.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2224-3 | 72162222403 | 30 CAPSULE in 1 BOTTLE (72162-2224-3) | 30 capsule | 2024-01-26 | No | No | Current |