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    VALIDUS PHARMS

    U.S.A
    ICHH-25
    Not Confirmed
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    VALIDUS PHARMS

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    BENAZEPRIL HYDROCHLORIDE

    Brand Name : LOTENSIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 1991-06-25

    Application Number : 19851

    Regulatory Info : RX

    Registration Country : USA

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    27

    VALIDUS PHARMS

    U.S.A
    ICHH-25
    Not Confirmed
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    VALIDUS PHARMS

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : LOTENSIN HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG;6.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1992-05-19

    Application Number : 20033

    Regulatory Info : DISCN

    Registration Country : USA

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    28

    VALIDUS PHARMS

    U.S.A
    ICHH-25
    Not Confirmed
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    VALIDUS PHARMS

    U.S.A
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    ICHH-25
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    Regulatory Info : RX

    Registration Country : USA

    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : LOTENSIN HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG;12.5MG

    Packaging :

    Approval Date : 1992-05-19

    Application Number : 20033

    Regulatory Info : RX

    Registration Country : USA

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    29

    VALIDUS PHARMS

    U.S.A
    ICHH-25
    Not Confirmed
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    VALIDUS PHARMS

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    ICHH-25
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : LOTENSIN HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG;25MG

    Packaging :

    Approval Date : 1992-05-19

    Application Number : 20033

    Regulatory Info : RX

    Registration Country : USA

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    30

    VALIDUS PHARMS

    U.S.A
    ICHH-25
    Not Confirmed
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    VALIDUS PHARMS

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : LOTENSIN HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG;12.5MG

    Packaging :

    Approval Date : 1992-05-19

    Application Number : 20033

    Regulatory Info : RX

    Registration Country : USA

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