Dofetilide (Mayne Pharma Inc.)
Welcome to the PulseAid listing for the Dofetilide drug offered from Mayne Pharma Inc.. This Antiarrhythmic [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: | Mayne Pharma Inc. |
| NON-PROPRIETARY NAME: | Dofetilide |
| SUBSTANCE NAME: | DOFETILIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Antiarrhythmic [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-06-07 |
| END MARKETING DATE: | 0000-00-00 |
Dofetilide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Dofetilide from Mayne Pharma Inc. |
| LABELER NAME: | Mayne Pharma Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 0.5(mg/1) |
| START MARKETING DATE: | 2016-06-07 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51862-005_9ef855ed-9897-4d05-9490-29a004a2e026 |
| PRODUCT NDC: | 51862-005 |
| APPLICATION NUMBER: | ANDA207058 |
Other DOFETILIDE Pharmaceutical Manufacturers / Labelers: