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    Approved Drug Products containing 211626 listed in the FDA Orange Book. Original Data : FDA Website

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    Graviti Pharmaceuticals

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    01 GRAVITI PHARMS (2)

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    01 CAPSULE, DELAYED RELEASE;ORAL (2)

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    01 RX (2)

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    01 FENOFIBRIC ACID (2)

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      CHOLINE FENOFIBRATE

      PDF Supplier PDF
      URL Supplier Web Content
      CAPSULE, DELAYED R...
      EQ 45MG FENOFIBRIC...
      2019-07-18
      211626
      FENOFIBRIC ACID
      RX
      No
      AB
      ASK
      US
      PHARMACOMPASS
      Upload
      your Marketing & Sales content
      Contact Supplier
        Virtual Booth Upload your Marketing & Sales content on your company Virtual Booth, click HERE
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        Flag India
        Virtual Booth Virtual Booth
        Digital Content Digital Content

        CHOLINE FENOFIBRATE

        PDF Supplier PDF
        URL Supplier Web Content
        CAPSULE, DELAYED R...
        EQ 135MG FENOFIBRI...
        2019-07-18
        211626
        FENOFIBRIC ACID
        RX
        No
        AB
        ASK
        US
        PHARMACOMPASS
        Upload
        your Marketing & Sales content

        Looking for FDA Orange Book APPLICATION 211626

        Looking for FDA Orange Book APPLICATION 211626 2

        19

        Graviti Pharmaceuticals, based in India, is a pharmaceutical company.

        One of their notable products is CHOLINE FENOFIBRATE, with a corresponding application number 211626.

        Regulatory Information RX

        With a dosage strength EQ 45MG FENOFIBRIC ACID

        Dosage Form Route CAPSULE, DELAYED RELEASE; ORAL

        Reference Listed Drug No

        Approved since 2019-07-18

        Therapeutic Equivalence (TE) Code AB

        18

        Graviti Pharmaceuticals, based in India, is a pharmaceutical company.

        One of their notable products is CHOLINE FENOFIBRATE, with a corresponding application number 211626.

        Regulatory Information RX

        With a dosage strength EQ 135MG FENOFIBRIC ACID

        Dosage Form Route CAPSULE, DELAYED RELEASE; ORAL

        Reference Listed Drug No

        Approved since 2019-07-18

        Therapeutic Equivalence (TE) Code AB

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