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    Epoprostenol Sodium

    ACTIVE PHARMA INGREDIENTS

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    01 2GLAXOSMITHKLINE INC

    02 2JANSSEN INC

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    JANSSEN INC

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    JANSSEN INC

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Prescription

    Registration Country : Canada

    EPOPROSTENOL (EPOPROSTENOL SODIUM)

    Brand Name : CARIPUL

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 0.5MG/VIAL

    Packaging : 10ML

    Approval Date :

    Application Number : 2397447

    Regulatory Info : Prescription

    Registration Country : Canada

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    02

    JANSSEN INC

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    JANSSEN INC

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Prescription

    Registration Country : Canada

    EPOPROSTENOL (EPOPROSTENOL SODIUM)

    Brand Name : CARIPUL

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 1.5MG/VIAL

    Packaging : 10ML

    Approval Date :

    Application Number : 2397455

    Regulatory Info : Prescription

    Registration Country : Canada

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    03

    GLAXOSMITHKLINE INC

    United Kingdom
    euroPLX 86 Munich
    Not Confirmed
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    GLAXOSMITHKLINE INC

    United Kingdom
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    euroPLX 86 Munich
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    Regulatory Info : Prescription

    Registration Country : Canada

    EPOPROSTENOL (EPOPROSTENOL SODIUM)

    Brand Name : FLOLAN

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 0.5MG/VIAL

    Packaging : 0.5 MG VIAL

    Approval Date :

    Application Number : 2230845

    Regulatory Info : Prescription

    Registration Country : Canada

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    04

    GLAXOSMITHKLINE INC

    United Kingdom
    euroPLX 86 Munich
    Not Confirmed
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    GLAXOSMITHKLINE INC

    United Kingdom
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    euroPLX 86 Munich
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Prescription

    Registration Country : Canada

    EPOPROSTENOL (EPOPROSTENOL SODIUM)

    Brand Name : FLOLAN

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 1.5MG/VIAL

    Packaging : 1.5 MG VIAL

    Approval Date :

    Application Number : 2230848

    Regulatory Info : Prescription

    Registration Country : Canada

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