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    Maralixibat Chloride

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    01 6Mirum Pharmaceuticals

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    01

    Mirum Pharmaceuticals

    U.S.A
    Pharmex
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    Mirum Pharmaceuticals

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    MARALIXIBAT CHLORIDE

    Brand Name : LIVMARLI

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 9.5MG BASE/ML

    Packaging :

    Approval Date : 2021-09-29

    Application Number : 214662

    Regulatory Info : RX

    Registration Country : USA

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    02

    Mirum Pharmaceuticals

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    Mirum Pharmaceuticals

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    Regulatory Info : RX

    Registration Country : USA

    MARALIXIBAT CHLORIDE

    Brand Name : LIVMARLI

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 19MG BASE/ML

    Packaging :

    Approval Date : 2024-07-24

    Application Number : 214662

    Regulatory Info : RX

    Registration Country : USA

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    03

    Mirum Pharmaceuticals

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    Regulatory Info : RX

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    MARALIXIBAT CHLORIDE

    Brand Name : LIVMARLI

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 2025-04-10

    Application Number : 219485

    Regulatory Info : RX

    Registration Country : USA

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    04

    Mirum Pharmaceuticals

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    Regulatory Info : RX

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    MARALIXIBAT CHLORIDE

    Brand Name : LIVMARLI

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 15MG BASE

    Packaging :

    Approval Date : 2025-04-10

    Application Number : 219485

    Regulatory Info : RX

    Registration Country : USA

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    05

    Mirum Pharmaceuticals

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    Mirum Pharmaceuticals

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    Regulatory Info : RX

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    MARALIXIBAT CHLORIDE

    Brand Name : LIVMARLI

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2025-04-10

    Application Number : 219485

    Regulatory Info : RX

    Registration Country : USA

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    06

    Mirum Pharmaceuticals

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    Mirum Pharmaceuticals

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    Regulatory Info : RX

    Registration Country : USA

    MARALIXIBAT CHLORIDE

    Brand Name : LIVMARLI

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 30MG BASE

    Packaging :

    Approval Date : 2025-04-10

    Application Number : 219485

    Regulatory Info : RX

    Registration Country : USA

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