FDA Approves New AGGRASTAT® Product Format

Bolus Vial to Improve Delivery Convenience

WINNIPEG., Medicure Inc., a specialty pharmaceutical company, announced that it has received approval from the U.S. Food and Drug Administration (FDA) for its new "bolus vial" product format for AGGRASTAT® (tirofiban HCl). 

The newly approved product format is a concentrated, pre-mixed, 15 ml vial designed specifically for convenient delivery of the AGGRASTAT bolus dose (25 mcg/kg). Development of the bolus vial was in response to feedback from interventional cardiologists and catheterization lab nurses from across the United States. 

Commercial release of the bolus vial will take place at the beginning of the fourth quarter of this year. The Company believes this new product format will have a positive impact on hospital utilization of AGGRASTAT. 

About Medicure Inc. 

Medicure is a specialty pharmaceutical company focused on the development and commercialization of therapeutics for the U.S. hospital market. The primary focus of the Company and its subsidiaries is the marketing and distribution of AGGRASTAT (tirofiban HCl) for non-ST elevation acute coronary syndrome in the United States, where it is sold through the Company's U.S. subsidiary, Medicure Pharma, Inc.  For more information on Medicure please visit www.medicure.com. 

About AGGRASTAT 

AGGRASTAT is indicated to reduce the rate of thrombotic cardiovascular events (combined endpoint of death, myocardial infarction, or refractory ischemia/repeat cardiac procedure) in patients with non-ST elevation acute coronary syndrome (NSTE-ACS). 

Source: Medicure Inc.