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    Approved Drug Products containing 210705 listed in the FDA Orange Book. Original Data : FDA Website

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    Ajanta Pharma Limited

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    01 AJANTA PHARMA LTD (3)

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    01 CAPSULE;ORAL (3)

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    01 FENOFIBRATE (MICRONIZED) (3)

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    FENOFIBRATE

    PDF Supplier PDF
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    CAPSULE; ORAL
    134MG
    2018-09-10
    210705
    FENOFIBRATE (MICRO...
    RX
    No
    AB
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    FENOFIBRATE

    PDF Supplier PDF
    URL Supplier Web Content
    CAPSULE; ORAL
    200MG
    2018-09-10
    210705
    FENOFIBRATE (MICRO...
    RX
    No
    AB
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    your Marketing & Sales content
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    • FDA
    • EDQM
    • WHO-GMP
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    FENOFIBRATE

    PDF Supplier PDF
    URL Supplier Web Content
    CAPSULE; ORAL
    67MG
    2018-09-10
    210705
    FENOFIBRATE (MICRO...
    RX
    No
    AB
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    PHARMACOMPASS
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    your Marketing & Sales content

    Looking for FDA Orange Book APPLICATION 210705

    Looking for FDA Orange Book APPLICATION 210705 3

    19

    Ajanta Pharma Limited, based in India, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is FENOFIBRATE, with a corresponding application number 210705.

    Regulatory Information RX

    With a dosage strength 134MG

    Dosage Form Route CAPSULE; ORAL

    Reference Listed Drug No

    Approved since 2018-09-10

    Therapeutic Equivalence (TE) Code AB

    18

    Ajanta Pharma Limited, based in India, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is FENOFIBRATE, with a corresponding application number 210705.

    Regulatory Information RX

    With a dosage strength 200MG

    Dosage Form Route CAPSULE; ORAL

    Reference Listed Drug No

    Approved since 2018-09-10

    Therapeutic Equivalence (TE) Code AB

    17

    Ajanta Pharma Limited, based in India, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is FENOFIBRATE, with a corresponding application number 210705.

    Regulatory Information RX

    With a dosage strength 67MG

    Dosage Form Route CAPSULE; ORAL

    Reference Listed Drug No

    Approved since 2018-09-10

    Therapeutic Equivalence (TE) Code AB

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