Hexalen (Eisai Inc.)
Welcome to the PulseAid listing for the Hexalen drug offered from Eisai Inc.. This Alkylating Activity [MoA],Alkylating Drug [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: | Eisai Inc. |
| NON-PROPRIETARY NAME: | altretamine |
| SUBSTANCE NAME: | ALTRETAMINE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Alkylating Activity [MoA],Alkylating Drug [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1990-12-26 |
| END MARKETING DATE: | 0000-00-00 |
Hexalen HUMAN PRESCRIPTION DRUG Details:
| Item Description | Hexalen from Eisai Inc. |
| LABELER NAME: | Eisai Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50(mg/1) |
| START MARKETING DATE: | 1990-12-26 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62856-001_81007003-bba4-467e-b643-08f1101258c9 |
| PRODUCT NDC: | 62856-001 |
| APPLICATION NUMBER: | NDA019926 |
Other ALTRETAMINE Pharmaceutical Manufacturers / Labelers:
