Mylotarg (Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.)
Welcome to the PulseAid listing for the Mylotarg drug offered from Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.. This CD33-directed Cytotoxin [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: | Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
NON-PROPRIETARY NAME: | gemtuzumab ozogamicin |
SUBSTANCE NAME: | GEMTUZUMAB OZOGAMICIN |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | CD33-directed Cytotoxin [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
MARKETING CATEGORY NAME: | BLA |
START MARKETING DATE: | 2017-09-07 |
END MARKETING DATE: | 0000-00-00 |
Mylotarg HUMAN PRESCRIPTION DRUG Details:
Item Description | Mylotarg from Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
LABELER NAME: | Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5(mg/5mL) |
START MARKETING DATE: | 2017-09-07 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0008-4510_da94b46a-1ee4-476a-bd6f-e60c52918c52 |
PRODUCT NDC: | 0008-4510 |
APPLICATION NUMBER: | BLA761060 |
Other GEMTUZUMAB OZOGAMICIN Pharmaceutical Manufacturers / Labelers: