Tretinoin 51672-1395
Product NDC
51672-1395- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- January 22, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA211645
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Tretinoin | 1 mg/g |
Drug Class
Retinoid [EPC]Retinoid [EPC]Retinoids [CS]
Packaging Options(2)
1 TUBE in 1 CARTON (51672-1395-0) / 20 g in 1 TUBE
1 TUBE in 1 CARTON (51672-1395-9) / 45 g in 1 TUBE