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    Momelotinib Hydrochloride

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    Regulatory Info : Approved

    Registration Country : Sweden

    Momelotinib Dihydrochloride Monohydrate

    Brand Name : Omjjara

    Dosage Form : Film Coated Tablet

    Dosage Strength : 100mg

    Packaging :

    Approval Date : 25/01/2024

    Application Number : 20221110000030

    Regulatory Info : Approved

    Registration Country : Sweden

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    Regulatory Info : Approved

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    Momelotinib Dihydrochloride Monohydrate

    Brand Name : Omjjara

    Dosage Form : Film Coated Tablet

    Dosage Strength : 150mg

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    Approval Date : 25/01/2024

    Application Number : 20221110000047

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    Regulatory Info : Approved

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    Momelotinib Dihydrochloride Monohydrate

    Brand Name : Omjjara

    Dosage Form : Film Coated Tablet

    Dosage Strength : 200mg

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    Approval Date : 25/01/2024

    Application Number : 20221110000054

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    Regulatory Info : Marketed

    Registration Country : Norway

    Momelotinib dihydrochloride monohydrate

    Brand Name : Omjjara

    Dosage Form : Film Coated Tablet

    Dosage Strength : 100mg

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    Regulatory Info : Marketed

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    Momelotinib dihydrochloride monohydrate

    Brand Name : Omjjara

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    Momelotinib dihydrochloride monohydrate

    Brand Name : Omjjara

    Dosage Form : Film Coated Tablet

    Dosage Strength : 200mg

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    Momelotinib Dihydrochloride Monohydrate

    Brand Name : Omjyara

    Dosage Form : Film Coated Tablet

    Dosage Strength : 100MG

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    Approval Date : 30-01-2024

    Application Number : 1231782001

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    Momelotinib Dihydrochloride Monohydrate

    Brand Name : Omjyara

    Dosage Form : Film Coated Tablet

    Dosage Strength : 150MG

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    Approval Date : 01-02-2024

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    Momelotinib Dihydrochloride Monohydrate

    Brand Name : Omjyara

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    Dosage Strength : 200MG

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    Approval Date : 30-01-2024

    Application Number : 1231782003

    Regulatory Info : Authorized

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    MOMELOTINIB (MOMELOTINIB DIHYDROCHLORIDE)

    Brand Name : OJJAARA

    Dosage Form : TABLET

    Dosage Strength : 100MG

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    Approval Date :

    Application Number : 2552965

    Regulatory Info : Prescription

    Registration Country : Canada

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    Brand Name : OJJAARA

    Dosage Form : TABLET

    Dosage Strength : 150MG

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    Momelotinib Dihydrochloride Monohydrate

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    Dosage Strength : 100mg

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    Approval Date : 25-01-2024

    Application Number : 28106871922

    Regulatory Info : Prescription

    Registration Country : Denmark

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    Approval Date : 25-01-2024

    Application Number : 28106872122

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    Approval Date : 25-01-2024

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