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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Landiolol Hydrochloride

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

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    01 1AOP Orphan

    02 2Fuji Pharma

    03 1Jiangsu Hengrui Medicine

    04 3Ono Pharmaceutical

    05 1TRIMEDIC THERAPEUTICS INC.

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    AOP Orphan

    Austria
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    Regulatory Info : RX

    Registration Country : USA

    LANDIOLOL HYDROCHLORIDE

    Brand Name : RAPIBLYK

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 280MG BASE/VIAL

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    Approval Date : 2024-11-22

    Application Number : 217202

    Regulatory Info : RX

    Registration Country : USA

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    Registration Country : Japan

    Landiolol Hydrochloride

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    Dosage Form : Powder for Injection

    Dosage Strength : 50MG

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    Registration Country : Japan

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    Registration Country : Japan

    Landiolol Hydrochloride

    Brand Name :

    Dosage Form : Powder for Injection

    Dosage Strength : 150MG

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    Registration Country : Japan

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    Registration Country : China

    Landiolol hydrochloride

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    Dosage Form : Injection

    Dosage Strength : 12.5MG

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    Registration Country : China

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    Ono Pharmaceutical

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    Registration Country : Japan

    Landiolol HCl

    Brand Name : Onoact

    Dosage Form : Intravenous Infusion

    Dosage Strength : 50MG

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    Registration Country : Japan

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    Ono Pharmaceutical

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    Registration Country : Japan

    Landiolol HCl

    Brand Name : Onoact

    Dosage Form : Intravenous Infusion

    Dosage Strength : 150MG

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    Approval Date :

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    Registration Country : Japan

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    Registration Country : Japan

    Landiolol HCl

    Brand Name : Corebeta

    Dosage Form : Powder for Injection

    Dosage Strength : 12.5MG

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    Registration Country : Japan

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    TRIMEDIC THERAPEUTICS INC.

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    Regulatory Info :

    Registration Country : Canada

    LANDIOLOL HYDROCHLORIDE

    Brand Name : SIBBORAN

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 300MG/VIAL

    Packaging :

    Approval Date :

    Application Number : 2543338

    Regulatory Info :

    Registration Country : Canada

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