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    TransoPharm USA works in the Sourcing and Management of Active Pharmaceutical Ingredients.

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    Metrochem Vortioxetine Hydrobromide

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.

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    Vortioxetine Hydrobromide

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    01 4ALKEM LABS LTD

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    04 4PRINSTON PHARMA INC

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    01

    ALKEM LABS LTD

    India
    USCC
    Not Confirmed
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    ALKEM LABS LTD

    India
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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date :

    Application Number : 211089

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    02

    CIPLA LTD

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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date :

    Application Number : 211085

    RX/OTC/DISCN :

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    TE Code :

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    03

    PRINSTON PHARMA INC

    U.S.A
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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date :

    Application Number : 211024

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    04

    PRINSTON PHARMA INC

    U.S.A
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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Approval Date :

    Application Number : 211024

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    05

    PRINSTON PHARMA INC

    U.S.A
    USCC
    Not Confirmed
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    PRINSTON PHARMA INC

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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

    Approval Date :

    Application Number : 211024

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    06

    PRINSTON PHARMA INC

    U.S.A
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    RLD :

    TE Code :

    VORTIOXETINE

    Brand Name : VORTIOXETINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Approval Date :

    Application Number : 211024

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    07

    TAKEDA PHARMS USA

    Japan
    USCC
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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 5MG BASE

    Approval Date : 2013-09-30

    Application Number : 204447

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    08

    TAKEDA PHARMS USA

    Japan
    USCC
    Not Confirmed
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    TAKEDA PHARMS USA

    Japan
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    USCC
    Not Confirmed
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    • EDQM
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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 :

    blank

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    09

    TAKEDA PHARMS USA

    Japan
    USCC
    Not Confirmed
    arrow

    TAKEDA PHARMS USA

    Japan
    arrow
    USCC
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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 :

    blank

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    10

    TAKEDA PHARMS USA

    Japan
    USCC
    Not Confirmed
    arrow

    TAKEDA PHARMS USA

    Japan
    arrow
    USCC
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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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 :

    blank

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