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Tretinoin
Tretinoin - 0187-1101-09 - (Tretinoin)
Drug Information of Tretinoin
| Product NDC: | 0187-1101 |
| Proprietary Name: | Tretinoin |
| Non Proprietary Name: | Tretinoin |
| Active Ingredient(s): | .05 g/100g & nbsp; Tretinoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tretinoin
| Product NDC: | 0187-1101 |
| Labeler Name: | Valeant Pharmaceuticals North America LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022070 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090801 |
Package Information of Tretinoin
| Package NDC: | 0187-1101-09 |
| Package Description: | 20 g in 1 TUBE (0187-1101-09) |
NDC Information of Tretinoin
| NDC Code | 0187-1101-09 |
| Proprietary Name | Tretinoin |
| Package Description | 20 g in 1 TUBE (0187-1101-09) |
| Product NDC | 0187-1101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tretinoin |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20090801 |
| Marketing Category Name | NDA |
| Labeler Name | Valeant Pharmaceuticals North America LLC |
| Substance Name | TRETINOIN |
| Strength Number | .05 |
| Strength Unit | g/100g |
| Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
