Rituxan (Genentech, Inc.)
Welcome to the PulseAid listing for the Rituxan 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: | rituximab |
SUBSTANCE NAME: | RITUXIMAB |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | CD20-directed Antibody Interactions [MoA],CD20-directed Cytolytic Antibody [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | BLA |
START MARKETING DATE: | 1997-11-26 |
END MARKETING DATE: | 0000-00-00 |
Rituxan HUMAN PRESCRIPTION DRUG Details:
Item Description | Rituxan from Genentech, Inc. |
LABELER NAME: | Genentech, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/mL) |
START MARKETING DATE: | 1997-11-26 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 50242-051_dbbf0d19-9518-4a12-a4e5-a5f77b005315 |
PRODUCT NDC: | 50242-051 |
APPLICATION NUMBER: | BLA103705 |
Other RITUXIMAB Pharmaceutical Manufacturers / Labelers: