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    Actavis Inc

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    ANAGRELIDE HYDROCHLORIDE

    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

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    Approval Date : 2005-04-18

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    Chartwell Pharmaceuticals llc

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    Cipla

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    Approval Date : 2005-04-18

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    Esjay Pharma

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    Dosage Form : CAPSULE;ORAL

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    Dosage Form : CAPSULE;ORAL

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    Approval Date : 2005-04-18

    Application Number : 76811

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    09

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    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 0.5MG BASE

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    Approval Date : 2005-04-18

    Application Number : 76910

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    10

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    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 1MG BASE

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    Rising Pharmaceuticals Inc

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    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 0.5MG BASE

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    Approval Date : 2006-06-27

    Application Number : 77613

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    Rising Pharmaceuticals Inc

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    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 1MG BASE

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    Approval Date : 2006-06-27

    Application Number : 77613

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    Registration Country : USA

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    13

    ROXANE

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    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 0.5MG BASE

    Packaging :

    Approval Date : 2005-04-18

    Application Number : 76489

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    Registration Country : USA

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    ROXANE

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    Brand Name : ANAGRELIDE HYDROCHLORIDE

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    Dosage Strength : EQ 1MG BASE

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    Takeda Pharmaceutical

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    Brand Name : AGRYLIN

    Dosage Form : CAPSULE;ORAL

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    Approval Date : 1997-03-14

    Application Number : 20333

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    Brand Name : AGRYLIN

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    Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1997-03-14

    Application Number : 20333

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    Torrent Pharmaceuticals Limited

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    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

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    Approval Date : 2017-06-30

    Application Number : 209151

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    Torrent Pharmaceuticals Limited

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    Brand Name : ANAGRELIDE HYDROCHLORIDE

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    Approval Date : 2017-06-30

    Application Number : 209151

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    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 0.5MG BASE

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    Approval Date : 2005-04-18

    Application Number : 76530

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    Registration Country : USA

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    BARR LABS

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    Brand Name : ANAGRELIDE HYDROCHLORIDE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 1MG BASE

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    Approval Date : 2005-04-18

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