Dermatop (Valeant Pharmaceuticals North America LLC)
Welcome to the PulseAid listing for the Dermatop drug offered from Valeant Pharmaceuticals North America LLC. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Valeant Pharmaceuticals North America LLC |
| NON-PROPRIETARY NAME: | prednicarbate |
| SUBSTANCE NAME: | PREDNICARBATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | CREAM |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1993-10-29 |
| END MARKETING DATE: | 0000-00-00 |
Dermatop HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dermatop from Valeant Pharmaceuticals North America LLC |
| LABELER NAME: | Valeant Pharmaceuticals North America LLC |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 1(mg/g) |
| START MARKETING DATE: | 1993-10-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0187-5182_ccc7985a-da29-475f-8a53-0f76ba20b86d |
| PRODUCT NDC: | 0187-5182 |
| APPLICATION NUMBER: | NDA020279 |
Other PREDNICARBATE Pharmaceutical Manufacturers / Labelers:
