Tretinoin
- Product NDC
- 50090-7171
- 11-digit product format
- 500907171
- Labeler code
- 50090
- Product ID
- 50090-7171_e078fd97-82cd-43fb-b32b-4ff103a76f92
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tretinoin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA215713
- Marketing category
- ANDA
- Marketing start
- 2023-01-05
- Substance
- TRETINOIN
- Active strength
- .25 mg/g
- 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 | .25 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5688UTC01R |
| Rxcui | 106302 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7171-0 | Tretinoin | 20 g in 1 TUBE | CREAM | 20 | | 1 |
| 50090-7171-0 | Tretinoin | 1 in 1 CARTON | CREAM | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7171 | TRETINOIN CREAM [A-S MEDICATION SOLUTIONS] | 1 | Current NDC, 2 package rows | 20240524_06ebaf8e-3648-493e-9b6a-9adef67bc65f.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 |
|---|
| 50090-7171-0 | 50090717100 | 1 TUBE in 1 CARTON (50090-7171-0) / 20 g in 1 TUBE | 1 tube | 2024-05-20 | No | No | Current |