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    Ibrutinib

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    Olpha

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    Virtual BoothOlpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.

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    Regulatory Info : Dossier Readiness: Q1 2026

    Registration Country : Latvia

    Ibrutinib

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    Regulatory Info : Dossier Readiness: Q1 2026

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    Pharmacyclics

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    Regulatory Info : RX

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    IBRUTINIB

    Brand Name : IMBRUVICA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 140MG

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    Approval Date : 2013-11-13

    Application Number : 205552

    Regulatory Info : RX

    Registration Country : USA

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    03

    NanoAlvand

    Iran
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    Virtual BoothNanoAlvand is the entrance to Global Markets as a trusted Highly Potent Products manufacturer.

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    Ibrutinib

    Brand Name : Bronib

    Dosage Form : Hard Gelatin Capsule

    Dosage Strength : 140MG

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    Registration Country : Iran

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    04

    Pharmacyclics

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    Regulatory Info : RX

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    IBRUTINIB

    Brand Name : IMBRUVICA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 70MG

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    Approval Date : 2017-12-20

    Application Number : 205552

    Regulatory Info : RX

    Registration Country : USA

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    05

    Pharmacyclics

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    Regulatory Info : RX

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    IBRUTINIB

    Brand Name : IMBRUVICA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 140MG

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    Approval Date : 2018-02-16

    Application Number : 210563

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    Pharmacyclics

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    Regulatory Info : RX

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    IBRUTINIB

    Brand Name : IMBRUVICA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 280MG

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    Approval Date : 2018-02-16

    Application Number : 210563

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    07

    Pharmacyclics

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    Regulatory Info : RX

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    IBRUTINIB

    Brand Name : IMBRUVICA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 420MG

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    Approval Date : 2018-02-16

    Application Number : 210563

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    Pharmacyclics

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    Regulatory Info : DISCN

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    IBRUTINIB

    Brand Name : IMBRUVICA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 560MG

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    Approval Date : 2018-02-16

    Application Number : 210563

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    Pharmacyclics

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    Regulatory Info : RX

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    IBRUTINIB

    Brand Name : IMBRUVICA

    Dosage Form : SUSPENSION;ORAL

    Dosage Strength : 70MG/ML

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    Approval Date : 2022-08-24

    Application Number : 217003

    Regulatory Info : RX

    Registration Country : USA

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    Pharmacyclics

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    Regulatory Info :

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    IBRUTINIB

    Brand Name : IMBRUVICA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 70MG

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    Approval Date :

    Application Number : 217003

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    Registration Country : USA

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    Pharmacyclics

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    Brand Name : IMBRUVICA

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 140MG

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    Application Number : 217003

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    Pharmacyclics

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    Brand Name : IMBRUVICA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 140MG

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    Application Number : 217003

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    Pharmacyclics

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    Regulatory Info :

    Registration Country : USA

    IBRUTINIB

    Brand Name : IMBRUVICA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 230MG

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    Application Number : 217003

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    Pharmacyclics

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    Regulatory Info :

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    Brand Name : IMBRUVICA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 420MG

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    Application Number : 217003

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    Registration Country : USA

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    Pharmacyclics

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    Regulatory Info :

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    Brand Name : IMBRUVICA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 560MG

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    Application Number : 217003

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    16

    Alvogen

    U.S.A
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    Registration Country : USA

    IBRUTINIB

    Brand Name : IBRUTINIB

    Dosage Form : TABLET;ORAL

    Dosage Strength : 140MG

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    Application Number : 212763

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    Sandoz B2B

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    Brand Name : IBRUTINIB

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    Application Number : 211267

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    Teva Pharmaceutical Industries

    Israel
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    Brand Name : IBRUTINIB

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    Dosage Strength : 140MG

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    Application Number : 211350

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    Zydus Lifesciences

    India
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    Regulatory Info : DISCN

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    Brand Name : IBRUTINIB

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 70MG

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    Approval Date : 2021-03-31

    Application Number : 211344

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    Zydus Lifesciences

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    Brand Name : IBRUTINIB

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    Dosage Strength : 140MG

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    Approval Date : 2021-03-31

    Application Number : 211344

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