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 DescriptionMylotarg from Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
LABELER NAME: Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.Mylotarg