Product NDC: | 54868-5510 |
Proprietary Name: | Clobex |
Non Proprietary Name: | clobetasol propionate |
Active Ingredient(s): | .5 mg/mL & nbsp; clobetasol propionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5510 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021835 |
Marketing Category: | NDA |
Start Marketing Date: | 20060123 |
Package NDC: | 54868-5510-0 |
Package Description: | 59 mL in 1 BOTTLE (54868-5510-0) |
NDC Code | 54868-5510-0 |
Proprietary Name | Clobex |
Package Description | 59 mL in 1 BOTTLE (54868-5510-0) |
Product NDC | 54868-5510 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clobetasol propionate |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20060123 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | CLOBETASOL PROPIONATE |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |