Gazyva

Active Ingredient(s): Obinutuzumab
FDA Approved: * November 1, 2013
Pharm Company: * GENENTECH
Category: Cancer

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Gazyva Overview

Obinutuzumab (called afutuzumab until 2009,[1] originally GA101) is a humanized anti-CD20 monoclonal antibody, originated by GlycArt Biotechnology AG and developed by Roche as a cancer treatment. It was approved under the trade name Gazyva by the US FDA in 2013, and as Gazyvaro by the EMA in Europe, for the treatment of chronic lymphocytic leukemia in combination with chemotherapy in treatment-naive patients, and as a second line treatment for follicular lymphoma. Contents...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Obinutuzumab

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Possible Dosages for this and Related Drugs:

Obinutuzumab
  • Injection: 1000mg/40ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Gazyva: (1 result)

Sorted by National Drug Code
  • 50242-070 Gazyva 1000 mg/40ml Intravenous Injection, Solution, Concentrate by Genentech, Inc.

Other drugs which contain Obinutuzumab or a similar ingredient: (1 result)




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