Product NDC: | 52544-044 |
Proprietary Name: | Cordran |
Non Proprietary Name: | Flurandrenolide |
Active Ingredient(s): | 4 ug/cm2 & nbsp; Flurandrenolide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | TAPE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52544-044 |
Labeler Name: | Watson Pharma, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA016455 |
Marketing Category: | NDA |
Start Marketing Date: | 19690729 |
Package NDC: | 52544-044-24 |
Package Description: | 450 cm2 in 1 CARTON (52544-044-24) |
NDC Code | 52544-044-24 |
Proprietary Name | Cordran |
Package Description | 450 cm2 in 1 CARTON (52544-044-24) |
Product NDC | 52544-044 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Flurandrenolide |
Dosage Form Name | TAPE |
Route Name | TOPICAL |
Start Marketing Date | 19690729 |
Marketing Category Name | NDA |
Labeler Name | Watson Pharma, Inc. |
Substance Name | FLURANDRENOLIDE |
Strength Number | 4 |
Strength Unit | ug/cm2 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |