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    Pharmaceuticals - Page 23

    Lupin launches Ethacrynic Acid Tablets USP, 25 mg

    Lupin launches Ethacrynic Acid Tablets USP, 25 mg

    Medical Dialogues Bureau26 Feb 2020 3:27 PM IST
    The product would be manufactured at Lupin's Nagpur OSD facility, India.
    Gileads drug leads global race to find virus treatment

    Gilead's drug leads global race to find virus treatment

    Medical Dialogues Bureau26 Feb 2020 2:24 PM IST
    Beijing | Tokyo: China will release results at the end of April from clinical trials of a Gilead Sciences drug that is emerging as a frontrunner in...
    Beximco Pharma announces Commercial Agreement with Mylan in Bangladesh

    Beximco Pharma announces Commercial Agreement with Mylan in Bangladesh

    Medical Dialogues Bureau25 Feb 2020 4:28 PM IST
    Beximco Pharmaceuticals Limited, manufacturer of generic pharmaceutical products and active pharmaceutical ingredients, has announced the signing of a...
    FDA authorizes marketing of the first genetic test for Fragile X Syndrome

    FDA authorizes marketing of the first genetic test for Fragile X Syndrome

    Medical Dialogues Bureau25 Feb 2020 2:09 PM IST
    US: The U.S. Food and Drug Administration has authorized marketing of the test to detect a genetic condition known as Fragile X Syndrome (FXS), the...
    Novartis announces FDA and EMA filing acceptance of ofatumumab, for treatment of relapsing form of MS

    Novartis announces FDA and EMA filing acceptance of ofatumumab, for treatment of relapsing form of MS

    Medical Dialogues Bureau25 Feb 2020 1:03 PM IST
    "With ofatumumab, we underpin our relentless dedication to reimagining medicine for patients across the MS spectrum and will work closely with the...
    BA/BE study applications have to be processed in 15 days: CDSCO

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

    Medical Dialogues Bureau25 Feb 2020 12:50 PM IST
    New Delhi: In order to streamline the applications process by various pharma companies, the CDSCO in its notice has recently mandated that BA/BE...
    Aurobindo Pharma gets USFDA nod for Azithromycin 250 mg and 500 mg

    Aurobindo Pharma gets USFDA nod for Azithromycin 250 mg and 500 mg

    Medical Dialogues Bureau24 Feb 2020 2:22 PM IST
    New Delhi: Drug firm Aurobindo Pharma has received final approval from the USFDA to manufacture and market Azithromycin tablets, used for the...
    USV not dominant player, hence no case: CCI dismisses petition by pharma wholesaler

    USV not dominant player, hence no case: CCI dismisses petition by pharma wholesaler

    MD bureau24 Feb 2020 1:23 PM IST
    New Delhi: Noting that the drug firm USV does not seem to enjoy the dominant position in the portfolio of medicines that it sells and hence no case...
    Coronavirus: Restrictions imposed on the export of medical equipment to China

    Coronavirus: Restrictions imposed on the export of medical equipment to China

    Medical Dialogues Bureau24 Feb 2020 12:29 PM IST
    New Delhi: India said some restrictions were imposed on export of certain medical equipment to China in view of their short supply within the country...
    Solara Puducherry and Mangalore facilities complete USFDA Inspection with zero 483s observations

    Solara Puducherry and Mangalore facilities complete USFDA Inspection with zero 483s observations

    Medical Dialogues Bureau24 Feb 2020 12:18 PM IST
    Chennai: Solara Active Pharma Science Limited (Solara), an active Pharmaceutical Ingredient provider has announced that the US Food and Drug...
    Biocons Insulin Manufacturing Facility in Malaysia Completes USFDA inspection with three observations

    Biocon's Insulin Manufacturing Facility in Malaysia Completes USFDA inspection with three observations

    Medical Dialogues Bureau24 Feb 2020 12:11 PM IST
    Malaysia:Drug major Biocon recently informed about the USFDA inspection at its Insulin Manufacturing Facility in Malaysia, and that the agency issued...
    USFDA approves Eli Lillys Trulicity (dulaglutide) for reduction in MACE in type 2 diabetes patient

    USFDA approves Eli Lilly's Trulicity (dulaglutide) for reduction in MACE in type 2 diabetes patient

    Medical Dialogues Bureau23 Feb 2020 12:00 PM IST
    New indication reflects a distinct patient population in the REWIND study, including primary people with multiple cardiovascular risk factors but...
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