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    IVAX Pharmaceuticals Inc

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    Brand Name : ISOSORBIDE MONONITRA...

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    Brand Name : ISOSORBIDE MONONITRA...

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    RLD : No

    TE Code :

    ISOSORBIDE MONONITRATE

    IVAX Pharmaceuticals Inc

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ISOSORBIDE MONONITRATE

    Dosage Strength : 120MG

    Approval Date : 2001-08-07

    Application Number : 75448

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : ISOSORBIDE MONONITRA...

    U.S.A
    BePharma
    Not Confirmed
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    Brand Name : ISOSORBIDE MONONITRA...

    U.S.A
    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.
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    RLD : No

    TE Code :

    ISOSORBIDE MONONITRATE

    IVAX Pharmaceuticals Inc

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ISOSORBIDE MONONITRATE

    Dosage Strength : 60MG

    Approval Date : 2000-06-19

    Application Number : 75448

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    Brand Name : ISOSORBIDE MONONITRA...

    U.S.A
    BePharma
    Not Confirmed
    arrow

    Brand Name : ISOSORBIDE MONONITRA...

    U.S.A
    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 U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    ISOSORBIDE MONONITRATE

    IVAX Pharmaceuticals Inc

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ISOSORBIDE MONONITRATE

    Dosage Strength : 30MG

    Approval Date : 2001-08-07

    Application Number : 75448

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.