Product NDC: | 68462-300 |
Proprietary Name: | Alclometasone Dipropionate |
Non Proprietary Name: | Alclometasone Dipropionate |
Active Ingredient(s): | .5 mg/g & nbsp; Alclometasone Dipropionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68462-300 |
Labeler Name: | Glenmark Generics Inc., USA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA079061 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090623 |
Package NDC: | 68462-300-47 |
Package Description: | 45 g in 1 TUBE (68462-300-47) |
NDC Code | 68462-300-47 |
Proprietary Name | Alclometasone Dipropionate |
Package Description | 45 g in 1 TUBE (68462-300-47) |
Product NDC | 68462-300 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Alclometasone Dipropionate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20090623 |
Marketing Category Name | ANDA |
Labeler Name | Glenmark Generics Inc., USA |
Substance Name | ALCLOMETASONE DIPROPIONATE |
Strength Number | .5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |