Tikosyn (Pfizer Laboratories Div Pfizer Inc)
Welcome to the PulseAid listing for the Tikosyn drug offered from Pfizer Laboratories Div Pfizer 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: | Pfizer Laboratories Div Pfizer Inc |
| NON-PROPRIETARY NAME: | dofetilide |
| SUBSTANCE NAME: | DOFETILIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Antiarrhythmic [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1999-10-01 |
| END MARKETING DATE: | 0000-00-00 |
Tikosyn HUMAN PRESCRIPTION DRUG Details:
| Item Description | Tikosyn from Pfizer Laboratories Div Pfizer Inc |
| LABELER NAME: | Pfizer Laboratories Div Pfizer Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.125(mg/1) |
| START MARKETING DATE: | 1999-10-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0069-5800_84580d57-01ac-4882-bcd5-2fd083378997 |
| PRODUCT NDC: | 0069-5800 |
| APPLICATION NUMBER: | NDA020931 |
Other DOFETILIDE Pharmaceutical Manufacturers / Labelers:
