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    ALISKIREN HEMIFUMARATE; AMLODIPINE BESYLATE

    Novartis Pharmaceuticals Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : TEKAMLO

    Dosage Strength : EQ 300MG BASE;EQ 5MG BAS...

    Approval Date : 2010-08-26

    Application Number : 22545

    RX/OTC/DISCN : DISCN

    RLD : No

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    Brand Name : TEKAMLO

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    RLD : No

    TE Code :

    ALISKIREN HEMIFUMARATE; AMLODIPINE BESYLATE

    Novartis Pharmaceuticals Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : TEKAMLO

    Dosage Strength : EQ 150MG BASE;EQ 5MG BAS...

    Approval Date : 2010-08-26

    Application Number : 22545

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Brand Name : TEKAMLO

    Switzerland
    BePharma
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    Brand Name : TEKAMLO

    Switzerland
    BePharma
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    ALISKIREN HEMIFUMARATE; AMLODIPINE BESYLATE

    Novartis Pharmaceuticals Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : TEKAMLO

    Dosage Strength : EQ 300MG BASE;EQ 10MG BA...

    Approval Date : 2010-08-26

    Application Number : 22545

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Product
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    Stock Recap
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    04

    Brand Name : TEKAMLO

    Switzerland
    BePharma
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    Brand Name : TEKAMLO

    Switzerland
    BePharma
    Not Confirmed
    arrow
    • 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.
    Post an Enquiry Post an Enquiry
    Flag Switzerland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    ALISKIREN HEMIFUMARATE; AMLODIPINE BESYLATE

    Novartis Pharmaceuticals Corporation

    Dosage Form : TABLET; ORAL

    Proprietary Name : TEKAMLO

    Dosage Strength : EQ 150MG BASE;EQ 10MG BA...

    Approval Date : 2010-08-26

    Application Number : 22545

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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