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    • Zydus Cadila gets...

    Zydus Cadila gets USFDA nod to market generic HIV treatment tablets

    Medical Dialogues BureauWritten by Medical Dialogues Bureau Published On 2018-11-17T11:45:55+05:30  |  Updated On 17 Nov 2018 11:45 AM IST
    Ahmedabad: Zydus Cadila has recently received the final approval from the USFDA to market Abacavir and Lamivudine Tablets USP, 600 mg/300 mg, and FondaparinuxSodium Injection USP, 2.5 mg/0.5 mL, 5 mg/0.4 mL 7.5 mg/0.6 mL and 10 mg/0.8 mL single-dose.

    Abacavir and Lamivudine Tablets are used with other antiretroviral medicines to treat Human Immunodeficiency Virus-type 1 (HIV-1) infection. HIV-1 is the virus that causes Acquired Immune Deficiency Syndrome (AIDS). It will be manufactured at the group’s formulations manufacturing facility at SEZ, Ahmedabad.

    Fondaparinux Injection is used to treat blood clots in deep veins (deep vein thrombosis) and the lungs (pulmonary embolism). It can also be used to prevent blood clots in patients undergoing certain types of surgeries. It will be manufactured at a partner’s manufacturing site.

    The group now has more than 230 approvals and has so far filed over 330 ANDAs since the
    commencement of the filing process in FY 2003-04.

    Read Also: Zydus Cadila gets USFDA nod for Anti-Fungal Ointment
    AbacavirAcquired Immune Deficiency SyndromeAIDSblood clotsFondaparinux InjectionHIV-1Human Immunodeficiency Virus-type 1Lamivudine TabletsZydus Cadila

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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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