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    Approved Drug Products containing 74514 listed in the FDA Orange Book. Original Data : FDA Website

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    Actavis Inc

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    01 ACTAVIS ELIZABETH (2)

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    01 TABLET, DELAYED RELEASE;ORAL (2)

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    01 DICLOFENAC SODIUM (2)

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    DICLOFENAC SODIUM

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    TABLET, DELAYED RE...
    75MG
    1996-03-26
    74514
    DICLOFENAC SODIUM
    RX
    No
    AB
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    DICLOFENAC SODIUM

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET, DELAYED RE...
    50MG
    1996-03-26
    74514
    DICLOFENAC SODIUM
    RX
    No
    AB
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    Looking for FDA Orange Book APPLICATION 74514

    Looking for FDA Orange Book APPLICATION 74514 2

    19

    Actavis Inc, based in Ireland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    One of their notable products is DICLOFENAC SODIUM, with a corresponding application number 74514.

    Regulatory Information RX

    With a dosage strength 75MG

    Dosage Form Route TABLET, DELAYED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 1996-03-26

    Therapeutic Equivalence (TE) Code AB

    18

    Actavis Inc, based in Ireland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    One of their notable products is DICLOFENAC SODIUM, with a corresponding application number 74514.

    Regulatory Information RX

    With a dosage strength 50MG

    Dosage Form Route TABLET, DELAYED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 1996-03-26

    Therapeutic Equivalence (TE) Code AB

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