Multaq
Active Ingredient(s): Dronedarone
First Approved by the FDA: July 1, 2009
Pharmaceutical Company: SANOFI AVENTIS US
Multaq Article Summary
Dronedarone (also Known As Sr33589 And Marketed As Multaq) Is A Drug By Sanofi-aventis, Mainly For The Indication Of Cardiac Arrhythmias (irregular Heartbeat). It Was Approved By The Fda On July 2, 2009. It Is Now Available As 400 mg Tablets In 60 Count Bottles. It Is Used For The Treatment Of Atrial Fibrillation And Atrial Flutter In Patients Whose Hearts Have Either Returned To Normal Rhythm Or Who Undergo Drug Therapy Or Electric Shock Treatment To Maintain Normal Rhythm.[1] However, The
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Tablet
400mg
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Dronedarone
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Drugs/Multaq.asp Last Updated November 16 2009
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