Desipramine Hydrochloride (Sandoz Inc)
Welcome to the PulseAid listing for the Desipramine Hydrochloride drug offered from Sandoz Inc. 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: | Sandoz Inc |
| NON-PROPRIETARY NAME: | Desipramine Hydrochloride |
| SUBSTANCE NAME: | DESIPRAMINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Tricyclic Antidepressant [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1988-05-24 |
| END MARKETING DATE: | 0000-00-00 |
Desipramine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Desipramine Hydrochloride from Sandoz Inc |
| LABELER NAME: | Sandoz Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 25(mg/1) |
| START MARKETING DATE: | 1988-05-24 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0781-1972_b29100b1-2813-4e85-ba28-d99df85aa522 |
| PRODUCT NDC: | 0781-1972 |
| APPLICATION NUMBER: | ANDA072100 |
Other DESIPRAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
