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    • FIRST: Mylan, Micro...

    FIRST: Mylan, Micro Labs get USFDA nod for generic version of blood thinner Eliquis

    Medical Dialogues BureauBy Medical Dialogues BureauPublished On 2019-12-24T09:45:05+05:30  |  Updated On 2021-08-18T15:47:48+05:30

    Sales of Eliquis, which Bristol-Myers co-developed with Pfizer, rose 22% to $1.93 billion and made up about 30% of the Bristol-Myers' total revenues in the latest reported quarter.


    New Delhi: The U.S. Food and Drug Administration said on Monday it has approved the first generic version of Bristol-Myers Squibb Co and Pfizer Inc's blood thinner Eliquis.


    The approval was granted to Micro Labs Ltd and Mylan Pharmaceuticals Inc, the agency said.


    Sales of Eliquis, which Bristol-Myers co-developed with Pfizer, rose 22% to $1.93 billion and made up about 30% of the Bristol-Myers' total revenues in the latest reported quarter.


    Read Also: Patent Infringement: Bristol-Myers wins case against Gilead; awarded USD 752 million in damages


    Eliquis is an approved treatment to reduce the risk of stroke in patients with irregular heartbeat or atrial fibrillation.


    The drug is also used to prevent blood clots in veins located deep in the body and in lungs.


    Read Also: Bristol-Myers, bluebird cancer therapy meets goal in mid-stage trial

    blood clot prevention blood thinner BMS ​Bristol Myers Squibb Bristol-Myers Bristol-Myers Squibb Co Eliquis Micro Labs Mylan Pfizer pharma pharma company pharma news USFDA 
    Source : Reuters

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    Medical Dialogues Bureau
    Medical Dialogues Bureau

      Medical Dialogues Bureau consists of a team of passionate medical/scientific writers, led by doctors and healthcare researchers.  Our team efforts to bring you updated and timely news about the important happenings of the medical and healthcare sector. Our editorial team can be reached at editorial@medicaldialogues.in. Check out more about our bureau/team here

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