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Prednicarbate
Prednicarbate - 0168-0410-60 - (prednicarbate)
Drug Information of Prednicarbate
| 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) |
Labeler Information of Prednicarbate
| 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 Information of Prednicarbate
| Package NDC: | 0168-0410-60 |
| Package Description: | 60 g in 1 TUBE (0168-0410-60) |
NDC Information of Prednicarbate
| NDC Code | 0168-0410-60 |
| Proprietary Name | Prednicarbate |
| Package Description | 60 g in 1 TUBE (0168-0410-60) |
| 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] |
