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    Aleor Derma Karakhadi unit clears USFDA inspection

    Medical Dialogues BureauWritten by Medical Dialogues Bureau Published On 2020-01-09T13:33:33+05:30  |  Updated On 9 Jan 2020 1:33 PM IST

    Mumbai: Drugmaker Alembic Pharma recently informed the bourses that its Joint Venture, Aleor Dermaceutical has successfully completed the US drug regulator's (USFDA) inspection.


    "Aleor Dermaceuticals Ltd. (Aleor Derma), a 60:40 Joint Venture between Alembic Pharmaceuticals Ltd. (Alembic) and Orbicular Pharmaceutical Technologies Pvt. Ltd. (Orbicular), has completed United States Food and Drug Administration (USFDA) inspection at its formulation manufacturing facility located at Karakhadi, Gujarat, India; without any observations, " Alembic said.


    Also Read: Alembic Pharma clears USFDA inspection at Bioequivalence facility in Vadodara


    The inspection was carried out from 6th January 2020 to 8th January 2020, it added.


    Alembic Pharmaceuticals is a vertically integrated research and development pharmaceutical company. Alembic has a cumulative total of 110 Abbreviated New Drug Application (ANDA) approvals (97 final approvals and 13 tentative approvals) from USFDA.


    Also Read: Alembic Pharma JV Aleor gets tentative USFDA nod for therapeutic equivalent of Pennsaid Topical Solution

    AlembicAlembic PharmaAleor dermaGujaratinspectionOrbicularpharmapharma newsUSFDA

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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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