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    Vortioxetine

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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date :

    Application Number : 211089

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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date :

    Application Number : 211085

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    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Approval Date :

    Application Number : 211024

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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

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    RLD : Yes

    TE Code :

    VORTIOXETINE HYDROBROMIDE

    Brand Name : TRINTELLIX

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Approval Date : 2013-09-30

    Application Number : 204447

    RX/OTC/DISCN : RX

    RLD : Yes

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    RLD : Yes

    TE Code :

    VORTIOXETINE HYDROBROMIDE

    Brand Name : TRINTELLIX

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2013-09-30

    Application Number : 204447

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    TAKEDA PHARMS USA

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    RLD : Yes

    TE Code :

    VORTIOXETINE HYDROBROMIDE

    Brand Name : TRINTELLIX

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 2013-09-30

    Application Number : 204447

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    TAKEDA PHARMS USA

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    RLD : Yes

    TE Code :

    VORTIOXETINE HYDROBROMIDE

    Brand Name : TRINTELLIX

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2013-09-30

    Application Number : 204447

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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