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    Eprosartan Mesylate

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    Regulatory Info : DISCN

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    EPROSARTAN MESYLATE

    Brand Name : TEVETEN

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1997-12-22

    Application Number : 20738

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    Registration Country : USA

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    EPROSARTAN MESYLATE

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    Dosage Strength : EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1997-12-22

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    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1999-05-27

    Application Number : 20738

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    EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE

    Brand Name : TEVETEN HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 600MG;12.5MG

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    Approval Date : 2001-11-01

    Application Number : 21268

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    EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE

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    Dosage Form : TABLET;ORAL

    Dosage Strength : 600MG;25MG

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    Approval Date : 2001-11-01

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    EPROSARTAN MESYLATE

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    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 400MG BASE

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    Approval Date : 2011-11-16

    Application Number : 202012

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    Approval Date : 2011-11-16

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