Prednicarbate (Oceanside Pharmaceuticals)
Welcome to the PulseAid listing for the Prednicarbate drug offered from Oceanside Pharmaceuticals. 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: | Oceanside Pharmaceuticals |
| NON-PROPRIETARY NAME: | emollient |
| 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 AUTHORIZED GENERIC |
| START MARKETING DATE: | 1993-10-29 |
| END MARKETING DATE: | 0000-00-00 |
Prednicarbate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Prednicarbate from Oceanside Pharmaceuticals |
| LABELER NAME: | Oceanside Pharmaceuticals |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1(mg/g) |
| START MARKETING DATE: | 1993-10-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68682-880_db10c116-5cac-4d50-92dd-250729d0ee3c |
| PRODUCT NDC: | 68682-880 |
| APPLICATION NUMBER: | NDA020279 |
Other PREDNICARBATE Pharmaceutical Manufacturers / Labelers:
