Iclusig

Active Ingredient(s): Ponatinib
FDA Approved: * December 14, 2012
Pharm Company: * ARIAD PHARMACEUTICALS
Category: Cancer

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

Iclusig Overview

Ponatinib (trade name Iclusig /aklus/ eye-KLOO-sig, previously AP24534) is an oral drug developed by ARIAD Pharmaceuticals for the treatment of chronic myeloid leukemia (CML) and Philadelphia chromosome–positive (Ph+) acute lymphoblastic leukemia (ALL). It is a multi-targeted tyrosine-kinase inhibitor.[2] Some forms of CML, those that have the T315I mutation, are resistant to current therapies such as imatinib. Ponatinib has been designed to be effective against these...

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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/Ponatinib

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NDC Database Records for Iclusig: (6 results)

Sorted by National Drug Code

• 63020-533 Iclusig 30 mg Oral Tablet, Film Coated by Millenium Pharmaceuticals Inc.
• 63020-534 Iclusig 45 mg Oral Tablet, Film Coated by Millenium Pharmaceuticals Inc.
• 63020-535 Iclusig 15 mg Oral Tablet, Film Coated by Millenium Pharmaceuticals Inc.
• 76189-533 Iclusig 30 mg Oral Tablet, Film Coated by Ariad Pharmaceuticals, Inc.
• 76189-534 Iclusig (As Ponatinib Hydrochloride) 45 mg Oral Tablet by Ariad Pharmaceuticals, Inc.
• 76189-535 Iclusig (As Ponatinib Hydrochloride) 15 mg Oral Tablet by Ariad Pharmaceuticals, Inc.

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

• PONATINIB