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    Iloprost

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    01

    ACTELION

    Switzerland
    Antibody Engineering
    Not Confirmed
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    ACTELION

    Switzerland
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    Antibody Engineering
    Not Confirmed
    • fda
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    RLD : No

    TE Code :

    ILOPROST

    Brand Name : VENTAVIS

    Dosage Form : SOLUTION;INHALATION

    Dosage Strength : 20MCG/2ML (10MCG/ML)

    Approval Date : 2004-12-29

    Application Number : 21779

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    ACTELION

    Switzerland
    Antibody Engineering
    Not Confirmed
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    ACTELION

    Switzerland
    arrow
    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    ILOPROST

    Brand Name : VENTAVIS

    Dosage Form : SOLUTION;INHALATION

    Dosage Strength : 10MCG/ML (10MCG/ML)

    Approval Date : 2005-12-08

    Application Number : 21779

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    03

    ACTELION

    Switzerland
    Antibody Engineering
    Not Confirmed
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    ACTELION

    Switzerland
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    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    ILOPROST

    Brand Name : VENTAVIS

    Dosage Form : SOLUTION;INHALATION

    Dosage Strength : 20MCG/ML (20MCG/ML)

    Approval Date : 2009-08-07

    Application Number : 21779

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    04

    BTG INTL

    U.S.A
    Antibody Engineering
    Not Confirmed
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    BTG INTL

    U.S.A
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    Antibody Engineering
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    RLD : Yes

    TE Code :

    ILOPROST

    Brand Name : AURLUMYN

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 100MCG/ML (100MCG/ML)

    Approval Date : 2024-02-13

    Application Number : 217933

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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