Tretinoin
- Product NDC
- 68071-3826
- 11-digit product format
- 680713826
- Labeler code
- 68071
- Product ID
- 68071-3826_31d2cd0d-3cb4-c719-e063-6294a90a2eb3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tretinoin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA211645
- Marketing category
- ANDA
- Marketing start
- 2019-01-22
- Substance
- TRETINOIN
- Active strength
- 1 mg/g
- Pharmacologic classes
- Retinoid [EPC], Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5688UTC01R | TRETINOIN | 302-79-4 | TRETINOIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3826-2 | 68071382602 | 1 TUBE in 1 CARTON (68071-3826-2) / 20 g in 1 TUBE | 1 tube | 2025-04-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tretinoin Cream USP, 0.1% | NuCare Pharmaceuticals, Inc. | 2025-04-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |