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 Description | Besponsa 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: | 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: