TRETINOIN
- Product NDC
- 70518-3233
- 11-digit product format
- 705183233
- Labeler code
- 70518
- Product ID
- 70518-3233_4ede161d-daeb-d892-e063-6294a90a7487
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tretinoin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075213
- Marketing category
- ANDA
- Marketing start
- 2021-10-11
- Substance
- TRETINOIN
- Active strength
- 1 mg/g
- Pharmacologic classes
- Retinoid [EPC], Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TRETINOIN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRETINOIN | 1 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5688UTC01R |
| Rxcui | 198300 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3233-0 | TRETINOIN | 20 g in 1 TUBE | CREAM | 20 | | 8 |
| 70518-3233-0 | TRETINOIN | 1 in 1 CARTON | CREAM | 1 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3233 | TRETINOIN CREAM [REMEDYREPACK INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20240316_c4d5155b-046d-4f94-bafc-651b572c2bd5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3233-0 | 70518323300 | 1 TUBE in 1 CARTON (70518-3233-0) / 20 g in 1 TUBE | 1 tube | 2021-10-11 | 0000-00-00 | No | No | Current |