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    Lumateperone Tosylate

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    01 3Intra-Cellular Therapies

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    01

    Intra-Cellular Therapies

    U.S.A
    The Generic Rx Session
    Not Confirmed
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    Intra-Cellular Therapies

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    LUMATEPERONE TOSYLATE

    Brand Name : CAPLYTA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 42MG BASE

    Packaging :

    Approval Date : 2019-12-20

    Application Number : 209500

    Regulatory Info : RX

    Registration Country : USA

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    02

    Intra-Cellular Therapies

    U.S.A
    The Generic Rx Session
    Not Confirmed
    arrow

    Intra-Cellular Therapies

    U.S.A
    arrow
    The Generic Rx Session
    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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    Regulatory Info : RX

    Registration Country : USA

    LUMATEPERONE TOSYLATE

    Brand Name : CAPLYTA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 10.5MG BASE

    Packaging :

    Approval Date : 2022-04-22

    Application Number : 209500

    Regulatory Info : RX

    Registration Country : USA

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    03

    Intra-Cellular Therapies

    U.S.A
    The Generic Rx Session
    Not Confirmed
    arrow

    Intra-Cellular Therapies

    U.S.A
    arrow
    The Generic Rx Session
    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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    Regulatory Info : RX

    Registration Country : USA

    LUMATEPERONE TOSYLATE

    Brand Name : CAPLYTA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 21MG BASE

    Packaging :

    Approval Date : 2022-04-22

    Application Number : 209500

    Regulatory Info : RX

    Registration Country : USA

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