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EPIDUO
EPIDUO - 0299-5908-02 - (adapalene and benzoyl peroxide)
Drug Information of EPIDUO
| 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) |
Labeler Information of EPIDUO
| 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 Information of EPIDUO
| Package NDC: | 0299-5908-02 |
| Package Description: | 2 g in 1 TUBE (0299-5908-02) |
NDC Information of EPIDUO
| NDC Code | 0299-5908-02 |
| Proprietary Name | EPIDUO |
| Package Description | 2 g in 1 TUBE (0299-5908-02) |
| 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] |
