Gazyva (Genentech, Inc.)


Welcome to the PulseAid listing for the Gazyva drug offered from Genentech, Inc.. This CD20-directed Antibody Interactions [MoA],CD20-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: Genentech, Inc.
NON-PROPRIETARY NAME: obinutuzumab
SUBSTANCE NAME: OBINUTUZUMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: CD20-directed Antibody Interactions [MoA],CD20-directed Cytolytic Antibody [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION, CONCENTRATE
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2013-11-01
END MARKETING DATE: 0000-00-00


Gazyva HUMAN PRESCRIPTION DRUG Details:

Item DescriptionGazyva from Genentech, Inc.
LABELER NAME: Genentech, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1000(mg/40mL)
START MARKETING DATE: 2013-11-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50242-070_ea9afb84-a9dd-4d98-831e-82c822ea57b4
PRODUCT NDC: 50242-070
APPLICATION NUMBER: BLA125486

Other OBINUTUZUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Genentech, Inc.Gazyva