Product NDC: | 0299-5908 |
Proprietary Name: | EPIDUO |
Non Proprietary Name: | adapalene and benzoyl peroxide |
Active Ingredient(s): | 1; 25 mg/g; mg/g & nbsp; adapalene and benzoyl peroxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0299-5908 |
Labeler Name: | Galderma Laboratories, L.P. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022320 |
Marketing Category: | NDA |
Start Marketing Date: | 20081208 |
Package NDC: | 0299-5908-25 |
Package Description: | 45 g in 1 BOTTLE, PUMP (0299-5908-25) |
NDC Code | 0299-5908-25 |
Proprietary Name | EPIDUO |
Package Description | 45 g in 1 BOTTLE, PUMP (0299-5908-25) |
Product NDC | 0299-5908 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | adapalene and benzoyl peroxide |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20081208 |
Marketing Category Name | NDA |
Labeler Name | Galderma Laboratories, L.P. |
Substance Name | ADAPALENE; BENZOYL PEROXIDE |
Strength Number | 1; 25 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |