Active Ingredient(s): Ofatumumab
FDA Approved: * October 26, 2009
Pharm Company: * GLAXO GRP LTD
Category: Cancer

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

Arzerra Overview

Ofatumumab,[9] sold under the brand name Arzerra among others, is a fully human monoclonal antibody to CD20, which appears to inhibit early-stage B lymphocyte activation. It is FDA approved for treating chronic lymphocytic leukemia that is refractory to fludarabine and alemtuzumab (Campath) and for the treatment of multiple sclerosis. It has also shown potential in treating follicular lymphoma, diffuse large B cell lymphoma, rheumatoid arthritis. Ofatumumab is the first market...

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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:

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Possible Dosages for this and Related Drugs:

  • Injection: 100mg/5ml
  • Solution: 20mg/0.4ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Arzerra: (4 results)

Sorted by National Drug Code
  • 0078-0669 Arzerra 20 mg/ml Intravenous Injection, Solution by Novartis Pharmaceuticals Corporation
  • 0078-0690 Arzerra 20 mg/ml Intravenous Injection, Solution by Novartis Pharmaceuticals Corporation
  • 0173-0821 Arzerra 20 mg/ml Intravenous Injection, Solution by Glaxosmithkline LLC
  • 63379-023 Arzerra 20 mg/ml Intravenous Injection, Solution by Glaxo Operations Uk Ltd

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

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