Product NDC: | 0187-5150 |
Proprietary Name: | Renova |
Non Proprietary Name: | Tretinoin |
Active Ingredient(s): | .2 mg/g & nbsp; Tretinoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0187-5150 |
Labeler Name: | Valeant Pharmaceuticals North America LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021108 |
Marketing Category: | NDA |
Start Marketing Date: | 20130415 |
Package NDC: | 0187-5150-02 |
Package Description: | 1 TUBE in 1 CARTON (0187-5150-02) > 2 g in 1 TUBE |
NDC Code | 0187-5150-02 |
Proprietary Name | Renova |
Package Description | 1 TUBE in 1 CARTON (0187-5150-02) > 2 g in 1 TUBE |
Product NDC | 0187-5150 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tretinoin |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130415 |
Marketing Category Name | NDA |
Labeler Name | Valeant Pharmaceuticals North America LLC |
Substance Name | TRETINOIN |
Strength Number | .2 |
Strength Unit | mg/g |
Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |