Product NDC: | 16590-033 |
Proprietary Name: | BETAMETHASONE CLOTRIMAZOLE |
Non Proprietary Name: | BETAMETHASONE CLOTRIMAZOLE |
Active Ingredient(s): | .64; 10 mg/1; mg/1 & nbsp; BETAMETHASONE CLOTRIMAZOLE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-033 |
Labeler Name: | Stat Rx USA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076002 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020802 |
Package NDC: | 16590-033-15 |
Package Description: | 1 CREAM in 1 CARTON (16590-033-15) |
NDC Code | 16590-033-15 |
Proprietary Name | BETAMETHASONE CLOTRIMAZOLE |
Package Description | 1 CREAM in 1 CARTON (16590-033-15) |
Product NDC | 16590-033 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | BETAMETHASONE CLOTRIMAZOLE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20020802 |
Marketing Category Name | ANDA |
Labeler Name | Stat Rx USA |
Substance Name | BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE |
Strength Number | .64; 10 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |