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
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 |
|---|
| 50090-7171-0 | 50090717100 | 1 TUBE in 1 CARTON (50090-7171-0) / 20 g in 1 TUBE | 1 tube | 2024-05-20 | No | No | Historical |