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    Mesoridazine Besylate

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    REF. STANDARDS & IMPURITIES

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    01

    NOVARTIS

    Switzerland
    PharmScience R&D
    Not Confirmed
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    NOVARTIS

    Switzerland
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    RLD : No

    TE Code :

    MESORIDAZINE BESYLATE

    Brand Name : SERENTIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 16774

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    NOVARTIS

    Switzerland
    PharmScience R&D
    Not Confirmed
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    NOVARTIS

    Switzerland
    arrow
    PharmScience R&D
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    MESORIDAZINE BESYLATE

    Brand Name : SERENTIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 16774

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    03

    NOVARTIS

    Switzerland
    PharmScience R&D
    Not Confirmed
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    NOVARTIS

    Switzerland
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    PharmScience R&D
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    MESORIDAZINE BESYLATE

    Brand Name : SERENTIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 16774

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    04

    NOVARTIS

    Switzerland
    PharmScience R&D
    Not Confirmed
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    NOVARTIS

    Switzerland
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    PharmScience R&D
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    MESORIDAZINE BESYLATE

    Brand Name : SERENTIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 16774

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    Website

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    05

    NOVARTIS

    Switzerland
    PharmScience R&D
    Not Confirmed
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    NOVARTIS

    Switzerland
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    PharmScience R&D
    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 : No

    TE Code :

    MESORIDAZINE BESYLATE

    Brand Name : SERENTIL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 25MG BASE/ML

    Approval Date : 1982-01-01

    Application Number : 16775

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    06

    NOVARTIS

    Switzerland
    PharmScience R&D
    Not Confirmed
    arrow

    NOVARTIS

    Switzerland
    arrow
    PharmScience R&D
    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 : No

    TE Code :

    MESORIDAZINE BESYLATE

    Brand Name : SERENTIL

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 25MG BASE/ML

    Approval Date : 1982-01-01

    Application Number : 16997

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

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