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    Fosinopril

    ACTIVE PHARMA INGREDIENTS

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    01 3ACTAVIS LABS FL INC

    02 4ANI PHARMS

    03 3APOTEX

    04 2AUROBINDO PHARMA

    05 3AUROBINDO PHARMA LTD

    06 5BRISTOL MYERS SQUIBB

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    01

    BRISTOL MYERS SQUIBB

    U.S.A
    Global ChemShow
    Not Confirmed
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    BRISTOL MYERS SQUIBB

    U.S.A
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    RLD : Yes

    TE Code :

    FOSINOPRIL SODIUM

    Brand Name : MONOPRIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1991-05-16

    Application Number : 19915

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    02

    BRISTOL MYERS SQUIBB

    U.S.A
    Global ChemShow
    Not Confirmed
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    BRISTOL MYERS SQUIBB

    U.S.A
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    RLD : Yes

    TE Code :

    FOSINOPRIL SODIUM

    Brand Name : MONOPRIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1991-05-16

    Application Number : 19915

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    03

    BRISTOL MYERS SQUIBB

    U.S.A
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    BRISTOL MYERS SQUIBB

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    RLD : Yes

    TE Code :

    FOSINOPRIL SODIUM

    Brand Name : MONOPRIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1995-03-28

    Application Number : 19915

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    04

    BRISTOL MYERS SQUIBB

    U.S.A
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    BRISTOL MYERS SQUIBB

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    RLD : Yes

    TE Code :

    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : MONOPRIL-HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1994-11-30

    Application Number : 20286

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    05

    BRISTOL MYERS SQUIBB

    U.S.A
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    BRISTOL MYERS SQUIBB

    U.S.A
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    RLD : Yes

    TE Code :

    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : MONOPRIL-HCT

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1994-11-30

    Application Number : 20286

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    TEVA

    Israel
    Global ChemShow
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    TEVA

    Israel
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    RLD : No

    TE Code : AB

    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Approval Date : 2003-11-25

    Application Number : 76139

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    TEVA

    Israel
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    TEVA

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    RLD : No

    TE Code : AB

    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Approval Date : 2003-11-25

    Application Number : 76139

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    TEVA

    Israel
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    TEVA

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    RLD : No

    TE Code : AB

    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

    Approval Date : 2003-11-25

    Application Number : 76139

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    UPSHER SMITH LABS

    U.S.A
    Global ChemShow
    Not Confirmed
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    UPSHER SMITH LABS

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    Global ChemShow
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    RLD : No

    TE Code :

    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Approval Date : 2004-10-08

    Application Number : 76188

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    UPSHER SMITH LABS

    U.S.A
    Global ChemShow
    Not Confirmed
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    UPSHER SMITH LABS

    U.S.A
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    Global ChemShow
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    RLD : No

    TE Code :

    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Approval Date : 2004-10-08

    Application Number : 76188

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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