Product NDC: | 51672-1262 |
Proprietary Name: | Desoximetasone |
Non Proprietary Name: | Desoximetasone |
Active Ingredient(s): | 2.5 mg/g & nbsp; Desoximetasone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51672-1262 |
Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074286 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960607 |
Package NDC: | 51672-1262-1 |
Package Description: | 1 TUBE in 1 CARTON (51672-1262-1) > 15 g in 1 TUBE |
NDC Code | 51672-1262-1 |
Proprietary Name | Desoximetasone |
Package Description | 1 TUBE in 1 CARTON (51672-1262-1) > 15 g in 1 TUBE |
Product NDC | 51672-1262 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Desoximetasone |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 19960607 |
Marketing Category Name | ANDA |
Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
Substance Name | DESOXIMETASONE |
Strength Number | 2.5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |