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    Zydus Cadila gets USFDA nod for Doxycycline Hyclate delayed-release tablets,Febuxostat tablets

    Medical Dialogues BureauWritten by Medical Dialogues Bureau Published On 24 Dec 2018 3:45 AM  |  Updated On 24 Dec 2018 3:45 AM
    Zydus Cadila gets USFDA nod for Doxycycline Hyclate delayed-release tablets,Febuxostat tablets




    New Delhi: Zydus Cadila has received final approval from the US health regulator to market Doxycycline Hyclate delayed-release tablets, used to treat bacterial infections.

    Zydus Cadila has received the final approval from the United States Food and Drug Administration (USFDA) to market the drug in the strengths of 75 mg, 100 mg and 150 mg, the company said in a BSE filing.

    Zydus Cadila said the drug will be produced at the group's formulations manufacturing facility at SEZ, Ahmedabad.

    The group has also received tentative approval for Febuxostat tablets in the strengths of 40 mg and 80 mg, used to treat hyperuricemia (constantly high levels of uric acid) in adults who have gout.

    The group has more than 241 approvals, and so far filed over 340 abbreviated new drug applications (ANDAs) since it started filings in 2003-04.

    Also Read: Zydus Cadila gets USFDA nod to market Albendazole Tablets



    abbreviated new drug applicationsANDAsBSEDoxycycline HyclateFebuxostat tabletsNew DelhiUnited States Food and Drug AdministrationUSFDAZydus Cadila
    Source : PTI

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    Medical Dialogues Bureau
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      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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