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    Approved Drug Products containing 211929 listed in the FDA Orange Book. Original Data : FDA Website

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    Sun Pharmaceutical Industries Limited

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    01 SUN PHARM INDS INC (2)

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    01 CAPSULE, DELAYED RELEASE;ORAL (2)

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    01 DISCN (2)

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    01 ORTIKOS (2)

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    01 Yes (2)

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    BUDESONIDE

    PDF Supplier PDF
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    CAPSULE, DELAYED R...
    6MG
    2019-06-13
    211929
    ORTIKOS
    DISCN
    Yes
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    • FDA
    • EDQM
    • WHO-GMP
    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

    BUDESONIDE

    PDF Supplier PDF
    URL Supplier Web Content
    CAPSULE, DELAYED R...
    9MG
    2019-06-13
    211929
    ORTIKOS
    DISCN
    Yes
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    US
    PHARMACOMPASS
    Upload
    your Marketing & Sales content

    Looking for FDA Orange Book APPLICATION 211929

    Looking for FDA Orange Book APPLICATION 211929 2

    19

    Sun Pharmaceutical Industries 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 BUDESONIDE, with a corresponding application number 211929.

    Regulatory Information DISCN

    With a dosage strength 6MG

    Dosage Form Route CAPSULE, DELAYED RELEASE; ORAL

    Reference Listed Drug Yes

    Approved since 2019-06-13

    18

    Sun Pharmaceutical Industries 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 BUDESONIDE, with a corresponding application number 211929.

    Regulatory Information DISCN

    With a dosage strength 9MG

    Dosage Form Route CAPSULE, DELAYED RELEASE; ORAL

    Reference Listed Drug Yes

    Approved since 2019-06-13

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