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Dermatop
Dermatop - 0066-0507-60 - (prednicarbate)
Drug Information of Dermatop
| Product NDC: | 0066-0507 |
| Proprietary Name: | Dermatop |
| 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 Dermatop
| Product NDC: | 0066-0507 |
| Labeler Name: | Dermik Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020279 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19931029 |
Package Information of Dermatop
| Package NDC: | 0066-0507-60 |
| Package Description: | 60 g in 1 TUBE (0066-0507-60) |
NDC Information of Dermatop
| NDC Code | 0066-0507-60 |
| Proprietary Name | Dermatop |
| Package Description | 60 g in 1 TUBE (0066-0507-60) |
| Product NDC | 0066-0507 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prednicarbate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19931029 |
| Marketing Category Name | NDA |
| Labeler Name | Dermik Laboratories |
| Substance Name | PREDNICARBATE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
