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    Lupin Tarapur API facility gets 3 observations from USFDA

    Medical Dialogues BureauWritten by Medical Dialogues Bureau Published On 2019-09-24T09:45:18+05:30  |  Updated On 24 Sept 2019 9:45 AM IST
    Lupin Tarapur API facility gets 3 observations from USFDA

    The inspection of the Tarapur facility was carried out by the US health regulator between September 16 to September 20, 2019, said Lupin.


    Mumbai: Pharma major Lupin Limited (Lupin) has received 3 observations from the United States Food and Drug Administration (U.S. FDA) for its Tarapur manufacturing (API) facility.


    The inspection of the facility was carried out by the US health regulator between September 16 to September 20, 2019. USFDA issues three observations after inspecting the facility.


    Commenting on the same, Lupin said, " The Company is confident of addressing them satisfactorily."


    Read Also: Lupin gets USFDA nod for a generic equivalent of UNITHROID to treat thyroid


    Based in Mumbai, Lupin is a player in the Cardiovascular, Diabetology, Asthma, Pediatric, CNS, Gl, Anti-Infective and NSAI D space and holds a global leadership position in the AntiTB segment.


    Read Also: Lupin gets USFDA warning letter for Mandideep Unit-1 facility

    APIBSELupinpharmapharma companypharma newspharma news indiaSEBITarapur facilityUSFDAUSFDA inspectionUSFDA observations

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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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