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Review Period Set for Eliquis
12/10/2015
 

Federal Register Notice: FDA has determined the regulatory review period for Bristol-Myers Squibb’s Eliquis is 3,685 days for the extension of a patent that claims the human drug product. Eliquis (apixaban) is indicated to reduce the risk of stroke and systemic embolism in patients with nonvalvular atrial fibrillation. To view this notice, click here.

 
 
 
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