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    Latest News - Page 105

    USFDA grants final nod to Caplin Point arm for Tranexamic Acid Injection

    USFDA grants final nod to Caplin Point arm for Tranexamic Acid Injection

    Medical Dialogues Bureau21 July 2019 9:45 AM IST
    Tranexamic Acid Injection is a generic therapeutic equivalent version of Cyklokapron Injection, 100 mg/ml, of Pharmacia & Upjohn Company.Chennai:...
    Teva Pharma wins USFDA approval for AirDuo Digihaler Inhalation Powder

    Teva Pharma wins USFDA approval for AirDuo Digihaler Inhalation Powder

    Medical Dialogues Bureau21 July 2019 9:30 AM IST
    Teva Pharma's AirDuo Digihaler is indicated for the treatment of asthma in patients aged 12 years and older. AirDuo Digihaler is not used to relieve...
    USFDA to review Sanofi isatuximab for treatment of multiple myeloma

    USFDA to review Sanofi isatuximab for treatment of multiple myeloma

    Medical Dialogues Bureau21 July 2019 9:15 AM IST
    Sanofi Isatuximab targets a specific epitope on the CD38 receptor. It is designed to trigger multiple, distinct mechanisms of action that are believed...
    JnJ, Oklahoma to wrap up first trial over opioid crisis

    JnJ, Oklahoma to wrap up first trial over opioid crisis

    Medical Dialogues Bureau21 July 2019 9:00 AM IST
    Lawyers for Attorney General Mike Hunter and JnJ are set to deliver closing arguments in state court in Norman, Oklahoma following six weeks of...
    Cipla gets 7 USFDA observations for Bengaluru API unit

    Cipla gets 7 USFDA observations for Bengaluru API unit

    Medical Dialogues Bureau20 July 2019 12:05 PM IST
    New Delhi: Drug firm Cipla recently said the US health regulator conducted an inspection at its API manufacturing facility in Virgonangar, Bengaluru...
    Dr Reddys unveils generic version of Allegra D in US to treat common cold, flu

    Dr Reddys unveils generic version of Allegra D in US to treat common cold, flu

    Medical Dialogues Bureau20 July 2019 11:37 AM IST
    In a BSE filing, Dr Reddy's Labs(Dr Reddys) announced "launch of Fexofenadine HCI 60 mg and Pseudoephedrine HCI 120 mg extended-release tablets, USP,...
    Novartis CEO sets aside 700 Million Dollar to settle doctor bribery lawsuit

    Novartis CEO sets aside 700 Million Dollar to settle doctor bribery lawsuit

    Medical Dialogues Bureau20 July 2019 9:52 AM IST
    ZURICH: Novartis Chief Executive Vas Narasimhan set aside $700 million to settle a U.S. doctor bribery lawsuit, as the Swiss drugmaker seeks to close...
    Gufic Biosciences to launch Botulinum Neuromedicine in India

    Gufic Biosciences to launch Botulinum Neuromedicine in India

    Medical Dialogues Bureau20 July 2019 9:15 AM IST
    Mumbai: Gufic Biosciences Limited ("the Company") recently announced to launch Botulinum Neurotoxin in India in collaboration with USA based Company...
    Bayer welcomes call for new trial in $2 billion glyphosate-based weedkiller case

    Bayer welcomes call for new trial in $2 billion glyphosate-based weedkiller case

    Medical Dialogues Bureau20 July 2019 9:00 AM IST
    Bayer had asked Judge Smith in June to overrule the jury verdict that its Roundup weedkiller caused the couple's non-Hodgkin's Lymphoma (NHL), arguing...
    Cabinet Nod to Rs 330 crore loan to 3 pharma PSUs for clearing staff liabilities

    Cabinet Nod to Rs 330 crore loan to 3 pharma PSUs for clearing staff liabilities

    Medical Dialogues Bureau19 July 2019 3:03 PM IST
    NEW DELHI: The Union Cabinet Wednesday approved loans of Rs 330.35 crore to three state-owned pharma companies to help them clear employees'...
    Abbott hits record high as blood sugar monitoring device- FreeStyle Libre 2 fuels profit

    Abbott hits record high as blood sugar monitoring device- FreeStyle Libre 2 fuels profit

    Medical Dialogues Bureau19 July 2019 3:02 PM IST
    Abbott Laboratories beat analysts' estimates for quarterly profit and lifted its full-year earnings forecast on Wednesday, boosted by a near 64% jump...
    Novartis key multiple sclerosis drug Gilenya® approved by China NMPA

    Novartis key multiple sclerosis drug Gilenya® approved by China NMPA

    Medical Dialogues Bureau19 July 2019 2:50 PM IST
    Basel: Chinese National Medical Products Administration (NMPA) approved Novartis's drug Gilenya® for relapsing forms of multiple sclerosis (RMS) for...
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    China offers tariff exemptions on US medical equipment amid virus outbreak

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    BA/BE study applications have to be processed in 15 days: CDSCO

    BA/BE study applications have to be processed in 15 days: CDSCO

    Mediclaim cannot be denied on presumption of pre-existing disease: NCDRC

    Mediclaim cannot be denied on presumption of pre-existing disease: NCDRC

    What Makes Group Medical Insurance Cheaper than Individual Insurance

    What Makes Group Medical Insurance Cheaper than Individual Insurance

    Drug marketers to take onus for quality of drugs, regulatory compliance: Health Ministry Gazette

    Drug marketers to take onus for quality of drugs, regulatory compliance: Health Ministry Gazette

    FDA expands approval of Gilenya to treat multiple sclerosis in pediatric patients

    FDA expands approval of Gilenya to treat multiple sclerosis in pediatric patients

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