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    moexipril hydrochloride

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    01 2APOTEX INC

    02 5CHARTWELL RX

    03 3GLENMARK PHARMS

    04 2GLENMARK PHARMS LTD

    05 3HERITAGE

    06 5TEVA

    07 5UCB INC

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    01

    TEVA

    Israel
    Medlab Asia & Asia Health
    Not Confirmed
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    TEVA

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    RLD : No

    TE Code : AB

    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG

    Approval Date : 2003-05-08

    Application Number : 76204

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    TEVA

    Israel
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    RLD : No

    TE Code : AB

    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

    Approval Date : 2003-05-08

    Application Number : 76204

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    TEVA

    Israel
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    RLD : No

    TE Code : AB

    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;7.5MG

    Approval Date : 2007-03-07

    Application Number : 76980

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    TEVA

    Israel
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    RLD : No

    TE Code : AB

    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG;15MG

    Approval Date : 2007-03-07

    Application Number : 76980

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    TEVA

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    RLD : No

    TE Code : AB

    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;15MG

    Approval Date : 2007-03-07

    Application Number : 76980

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    UCB INC

    Belgium
    Medlab Asia & Asia Health
    Not Confirmed
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    UCB INC

    Belgium
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    RLD : No

    TE Code :

    MOEXIPRIL HYDROCHLORIDE

    Brand Name : UNIVASC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1995-04-19

    Application Number : 20312

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    UCB INC

    Belgium
    Medlab Asia & Asia Health
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    RLD : No

    TE Code :

    MOEXIPRIL HYDROCHLORIDE

    Brand Name : UNIVASC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1995-04-19

    Application Number : 20312

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    UCB INC

    Belgium
    Medlab Asia & Asia Health
    Not Confirmed
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    UCB INC

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    Medlab Asia & Asia Health
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    RLD : No

    TE Code :

    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : UNIRETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1997-06-27

    Application Number : 20729

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    UCB INC

    Belgium
    Medlab Asia & Asia Health
    Not Confirmed
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    UCB INC

    Belgium
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    Medlab Asia & Asia Health
    Not Confirmed
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    RLD : No

    TE Code :

    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : UNIRETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1997-06-27

    Application Number : 20729

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    UCB INC

    Belgium
    Medlab Asia & Asia Health
    Not Confirmed
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    UCB INC

    Belgium
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    Medlab Asia & Asia Health
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    RLD : No

    TE Code :

    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : UNIRETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 2002-02-14

    Application Number : 20729

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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