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Adapalene
Adapalene - 51672-4155-6 - (Adapalene)
Drug Information of Adapalene
| Product NDC: | 51672-4155 |
| 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: | 51672-4155 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020380 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19960531 |
Package Information of Adapalene
| Package NDC: | 51672-4155-6 |
| Package Description: | 1 TUBE in 1 CARTON (51672-4155-6) > 45 g in 1 TUBE |
NDC Information of Adapalene
| NDC Code | 51672-4155-6 |
| Proprietary Name | Adapalene |
| Package Description | 1 TUBE in 1 CARTON (51672-4155-6) > 45 g in 1 TUBE |
| Product NDC | 51672-4155 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Adapalene |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19960531 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | ADAPALENE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |
