Ilaris

Active Ingredient(s): Canakinumab
FDA Approved: * June 17, 2009
Pharm Company: * NOVARTIS PHARMS
Category: Anti-Inflammatory

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



Ilaris Overview

Canakinumab (INN, trade name Ilaris, previously ACZ885)[2] is a human monoclonal antibody targeted at interleukin-1 beta. It has no cross-reactivity with other members of the interleukin-1 family, including interleukin-1 alpha.[3] Canakinumab was approved for the treatment of cryopyrin-associated periodic syndromes (CAPS) by the U.S. Food and Drug Administration (FDA) in June 2009[4] and by the European Medicines Agency in October 2009.[...

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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/Canakinumab

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Possible Dosages for this and Related Drugs:

Canakinumab
  • Injection: 180mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Ilaris: (2 results)

Sorted by National Drug Code
  • 0078-0582 Ilaris 150 mg/ml Subcutaneous Injection, Powder, Lyophilized, for Solution by Novartis Pharmaceuticals Corporation
  • 0078-0734 Ilaris 150 mg/ml Subcutaneous Injection, Solution by Novartis Pharmaceuticals Corporation

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

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