Amoxapine (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Amoxapine drug offered from Actavis Pharma, 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: | Actavis Pharma, Inc. |
| NON-PROPRIETARY NAME: | Amoxapine |
| SUBSTANCE NAME: | AMOXAPINE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Tricyclic Antidepressant [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1992-08-28 |
| END MARKETING DATE: | 0000-00-00 |
Amoxapine HUMAN PRESCRIPTION DRUG Details:
| Item Description | Amoxapine from Actavis Pharma, Inc. |
| LABELER NAME: | Actavis Pharma, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 25(mg/1) |
| START MARKETING DATE: | 1992-08-28 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0591-5713_5b94aa29-e270-4591-87c5-fa97e38c3b6b |
| PRODUCT NDC: | 0591-5713 |
| APPLICATION NUMBER: | ANDA072688 |
Other AMOXAPINE Pharmaceutical Manufacturers / Labelers:
