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    • Cipla gets USFDA nod...

    Cipla gets USFDA nod for lipid regulating tablets

    Written by supriya kashyap kashyap Published On 2016-12-20T11:18:41+05:30  |  Updated On 20 Dec 2016 11:18 AM IST

    New Delhi : Drug firm Cipla has received final approval from the US health regulator for lipid regulating Fenofibrate tablets.


    The company "has received final approval for its abbreviated new drug application (ANDA) for Fenofibrate tablets USP 48mg and 145mg, from the United States Food and Drug Administration (USFDA)," Cipla said in a BSE filing.


    The tablets are generic versions of AbbVie's Tricor tablets, it added.


    "Tricor tablets and generic equivalents had US sales of approximately USD 307 million for the 12-month period ending October 2016, according to IMS Health," Cipla said.


    The company's portfolio includes over 1,000 products across a wide range of therapeutic categories.


    Shares of Cipla were trading 0.76 per cent up at Rs 570.30 on BSE.

    Abbreviated New Drug ApplicationAbbVieANDACiplaFenofibratelipid regulatinglipid regulating tabletsUS Food & Drug AdministrationUSFDA
    Source : PTI

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    supriya kashyap kashyap
    supriya kashyap kashyap
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