Product NDC: | 0168-0410 |
Proprietary Name: | Prednicarbate |
Non Proprietary Name: | prednicarbate |
Active Ingredient(s): | 1 mg/g & nbsp; prednicarbate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0168-0410 |
Labeler Name: | E. Fougera & Co., a division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077236 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070309 |
Package NDC: | 0168-0410-15 |
Package Description: | 15 g in 1 TUBE (0168-0410-15) |
NDC Code | 0168-0410-15 |
Proprietary Name | Prednicarbate |
Package Description | 15 g in 1 TUBE (0168-0410-15) |
Product NDC | 0168-0410 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | prednicarbate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20070309 |
Marketing Category Name | ANDA |
Labeler Name | E. Fougera & Co., a division of Fougera Pharmaceuticals Inc. |
Substance Name | PREDNICARBATE |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |