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    Approval Date :

    Application Number : 207948

    Regulatory Info :

    Registration Country : USA

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    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    24

    Par Pharmaceutical

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Par Pharmaceutical

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info :

    Registration Country : USA

    LURASIDONE HYDROCHLORIDE

    Brand Name : LURASIDONE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 80MG

    Packaging :

    Approval Date :

    Application Number : 207948

    Regulatory Info :

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    25

    Par Pharmaceutical

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Par Pharmaceutical

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    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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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info :

    Registration Country : USA

    LURASIDONE HYDROCHLORIDE

    Brand Name : LURASIDONE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 120MG

    Packaging :

    Approval Date :

    Application Number : 207948

    Regulatory Info :

    Registration Country : USA

    blank

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    Digital Content

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    26

    Sunovion Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Sunovion Pharmaceuticals

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    LURASIDONE HYDROCHLORIDE

    Brand Name : LATUDA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 2010-10-28

    Application Number : 200603

    Regulatory Info : RX

    Registration Country : USA

    blank

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    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    27

    Sunovion Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Sunovion Pharmaceuticals

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    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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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    LURASIDONE HYDROCHLORIDE

    Brand Name : LATUDA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 80MG

    Packaging :

    Approval Date : 2010-10-28

    Application Number : 200603

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

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    28

    Sunovion Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Sunovion Pharmaceuticals

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    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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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    LURASIDONE HYDROCHLORIDE

    Brand Name : LATUDA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2011-12-07

    Application Number : 200603

    Regulatory Info : RX

    Registration Country : USA

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    Digital Content

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    29

    Sunovion Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Sunovion Pharmaceuticals

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    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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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    LURASIDONE HYDROCHLORIDE

    Brand Name : LATUDA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 120MG

    Packaging :

    Approval Date : 2012-04-26

    Application Number : 200603

    Regulatory Info : RX

    Registration Country : USA

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    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    30

    Sunovion Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Sunovion Pharmaceuticals

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    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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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    LURASIDONE HYDROCHLORIDE

    Brand Name : LATUDA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 60MG

    Packaging :

    Approval Date : 2013-07-12

    Application Number : 200603

    Regulatory Info : RX

    Registration Country : USA

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