Synribo

Active Ingredient(s): Omacetaxine Mepesuccinate
FDA Approved: * October 26, 2012
Pharm Company: * IVAX PHARMS
Category: Cancer

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

Synribo Overview

Omacetaxine mepesuccinate (INN, trade names Synribo ), formerly named as homoharringtonine or HHT, is a pharmaceutical drug substance that is indicated for treatment of chronic myeloid leukemia (CML). It is a natural product first discovered in Cephalotaxus harringtonii, now manufactured by hemi-synthesis. It was approved by the US FDA in October 2012 for the treatment of adult patients with CML with resistance and/or intolerance to two or more tyrosine kinase inhibitors (TKIs).[1&am...

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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/Omacetaxine_mepesuccinate

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NDC Database Records for Synribo: (1 result)

Sorted by National Drug Code

• 63459-177 Synribo 3.5 mg/ml Subcutaneous Injection, Powder, Lyophilized, for Solution by Cephalon, Inc.

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

• OMACETAXINE MEPESUCCINATE

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