Desipramine Hydrochloride (Winthrop U.S.)
Welcome to the PulseAid listing for the Desipramine Hydrochloride drug offered from Winthrop U.S.. This Tricyclic Antidepressant [EPC] 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: | Winthrop U.S. |
| NON-PROPRIETARY NAME: | desipramine hydrochloride |
| SUBSTANCE NAME: | DESIPRAMINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Tricyclic Antidepressant [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, SUGAR COATED |
| MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
| START MARKETING DATE: | 2014-04-01 |
| END MARKETING DATE: | 0000-00-00 |
Desipramine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Desipramine Hydrochloride from Winthrop U.S. |
| LABELER NAME: | Winthrop U.S. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 10(mg/1) |
| START MARKETING DATE: | 2014-04-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0955-1030_374a094f-5f1b-49a8-86a9-06780b524679 |
| PRODUCT NDC: | 0955-1030 |
| APPLICATION NUMBER: | NDA014399 |
Other DESIPRAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
