Besponsa (Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.)


Welcome to the PulseAid listing for the Besponsa drug offered from Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.. This 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: inotuzumab ozogamicin
SUBSTANCE NAME: INOTUZUMAB OZOGAMICIN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2017-08-18
END MARKETING DATE: 0000-00-00


Besponsa HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBesponsa from Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
LABELER NAME: Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.25(mg/mL)
START MARKETING DATE: 2017-08-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0008-0100_ee6c1ea5-47ab-478b-996d-461022339832
PRODUCT NDC: 0008-0100
APPLICATION NUMBER: BLA761040

Other INOTUZUMAB OZOGAMICIN Pharmaceutical Manufacturers / Labelers:

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