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Prednicarbate
Prednicarbate - 66993-880-15 - (Prednicarbate)
Drug Information of Prednicarbate
| Product NDC: | 66993-880 |
| Proprietary Name: | Prednicarbate |
| Non Proprietary Name: | Prednicarbate |
| Active Ingredient(s): | 1 mg/g & nbsp; Prednicarbate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prednicarbate
| Product NDC: | 66993-880 |
| Labeler Name: | Prasco Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020279 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20070430 |
Package Information of Prednicarbate
| Package NDC: | 66993-880-15 |
| Package Description: | 15 g in 1 TUBE (66993-880-15) |
NDC Information of Prednicarbate
| NDC Code | 66993-880-15 |
| Proprietary Name | Prednicarbate |
| Package Description | 15 g in 1 TUBE (66993-880-15) |
| Product NDC | 66993-880 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Prednicarbate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20070430 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Prasco Laboratories |
| Substance Name | PREDNICARBATE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
