Tretinoin
- Product NDC
- 72162-1220
- 11-digit product format
- 721621220
- Labeler code
- 72162
- Product ID
- 72162-1220_f882a775-5ca1-4aeb-868e-ab77e0f31875
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tretinoin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201687
- Marketing category
- ANDA
- Marketing start
- 2012-10-24
- Substance
- TRETINOIN
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tretinoin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRETINOIN | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5688UTC01R |
| Rxcui | 199159 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1220-1 | Tretinoin | 100 in 1 BOTTLE | CAPSULE | 100 | | 101 |
| 72162-1220-3 | Tretinoin | 30 in 1 BOTTLE | CAPSULE | 30 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1220 | TRETINOIN CAPSULE [BRYANT RANCH PREPACK] | 101 | Current NDC, 2 package rows | 20240718_7a7974c7-8b6c-41ae-9a48-a08a1439087a.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 |
|---|
| 72162-1220-1 | 72162122001 | 100 CAPSULE in 1 BOTTLE (72162-1220-1) | 100 capsule | 2024-02-09 | No | No | Historical |
| 72162-1220-3 | 72162122003 | 30 CAPSULE in 1 BOTTLE (72162-1220-3) | 30 capsule | 2024-02-09 | No | No | Historical |