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Adapalene
Adapalene - 0093-6301-95 - (Adapalene)
Drug Information of Adapalene
| Product NDC: | 0093-6301 |
| Proprietary Name: | Adapalene |
| Non Proprietary Name: | Adapalene |
| Active Ingredient(s): | 1 mg/g & nbsp; Adapalene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Adapalene
| Product NDC: | 0093-6301 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090962 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100602 |
Package Information of Adapalene
| Package NDC: | 0093-6301-95 |
| Package Description: | 45 g in 1 TUBE (0093-6301-95) |
NDC Information of Adapalene
| NDC Code | 0093-6301-95 |
| Proprietary Name | Adapalene |
| Package Description | 45 g in 1 TUBE (0093-6301-95) |
| Product NDC | 0093-6301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Adapalene |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100602 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | ADAPALENE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
