LEMTRADA (Genzyme Corporation)
Welcome to the PulseAid listing for the LEMTRADA drug offered from Genzyme Corporation. This CD52-directed Antibody Interactions [MoA],CD52-directed Cytolytic Antibody [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: | Genzyme Corporation |
| NON-PROPRIETARY NAME: | ALEMTUZUMAB |
| SUBSTANCE NAME: | ALEMTUZUMAB |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | CD52-directed Antibody Interactions [MoA],CD52-directed Cytolytic Antibody [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | BLA |
| START MARKETING DATE: | 2014-11-18 |
| END MARKETING DATE: | 0000-00-00 |
LEMTRADA HUMAN PRESCRIPTION DRUG Details:
| Item Description | LEMTRADA from Genzyme Corporation |
| LABELER NAME: | Genzyme Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 12(mg/1.2mL) |
| START MARKETING DATE: | 2014-11-18 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 58468-0200_347e46f8-486d-4626-ac47-5916d5bb3d4d |
| PRODUCT NDC: | 58468-0200 |
| APPLICATION NUMBER: | BLA103948 |
Other ALEMTUZUMAB Pharmaceutical Manufacturers / Labelers:
