Tretinoin
- Product NDC
- 68682-514
- 11-digit product format
- 686820514
- Labeler code
- 68682
- Product ID
- 68682-514_c4ef7e4d-9c2e-4022-b7ab-b55962c1a58a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tretinoin
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA020475
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-03-14
- Substance
- TRETINOIN
- Active strength
- .4 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 | .4 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5688UTC01R |
| Rxcui | 313453, 359050, 1488045 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68682-514 | TRETINOIN GEL [OCEANSIDE PHARMACEUTICALS] | 10 | Current NDC, Legacy NDC, 6 package rows | 20240410_d3c528d2-429d-4f37-9ebf-eee8b9fd3050.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 |
|---|
| 68682-514-92 | 68682051492 | 1 TUBE in 1 CARTON (68682-514-92) / 20 g in 1 TUBE | 1 tube | 2013-03-14 | 0000-00-00 | No | No | Current |
| 68682-514-94 | 68682051494 | 1 TUBE in 1 CARTON (68682-514-94) / 45 g in 1 TUBE | 1 tube | 2013-03-14 | 0000-00-00 | No | No | Current |
| 68682-514-95 | 68682051495 | 1 BOTTLE, PUMP in 1 CARTON (68682-514-95) / 50 g in 1 BOTTLE, PUMP | | 2013-03-14 | 0000-00-00 | No | No | Current |