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    Approved Drug Products containing Quinapril listed in the FDA Orange Book. Original Data : FDA Website

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    Quinapril

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    PRICE INFORMATION

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

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    01 4ACTAVIS ELIZABETH

    02 4ACTAVIS LABS FL INC

    03 4ANI PHARMS

    04 3APOTEX

    05 4APOTEX INC

    06 3AUROBINDO PHARMA

    07 4AUROBINDO PHARMA LTD

    08 7CHARTWELL RX

    09 7INVAGEN PHARMS

    10 4LUPIN

    11 4MYLAN

    12 7NORVIUM BIOSCIENCE

    13 7PFIZER PHARMS

    14 4PRINSTON INC

    15 11SUN PHARM INDS LTD

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    01

    ANI PHARMS

    U.S.A
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    ANI PHARMS

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    RLD : No

    TE Code :

    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Approval Date : 2007-08-24

    Application Number : 75504

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    ANI PHARMS

    U.S.A
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    RLD : No

    TE Code :

    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2007-08-24

    Application Number : 75504

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    ANI PHARMS

    U.S.A
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    ANI PHARMS

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    RLD : No

    TE Code :

    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2007-08-24

    Application Number : 75504

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    PFIZER PHARMS

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    RLD : Yes

    TE Code :

    QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCUPRIL

    Dosage Form : TABLET;ORAL

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

    Approval Date : 1991-11-19

    Application Number : 19885

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    05

    PFIZER PHARMS

    U.S.A
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    RLD : Yes

    TE Code :

    QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCUPRIL

    Dosage Form : TABLET;ORAL

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

    Approval Date : 1991-11-19

    Application Number : 19885

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    PFIZER PHARMS

    U.S.A
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    RLD : Yes

    TE Code :

    QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCUPRIL

    Dosage Form : TABLET;ORAL

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

    Approval Date : 1991-11-19

    Application Number : 19885

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    07

    PFIZER PHARMS

    U.S.A
    Luxepack
    Not Confirmed
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    PFIZER PHARMS

    U.S.A
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    RLD : Yes

    TE Code :

    QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCUPRIL

    Dosage Form : TABLET;ORAL

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

    Approval Date : 1991-11-19

    Application Number : 19885

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    08

    PFIZER PHARMS

    U.S.A
    Luxepack
    Not Confirmed
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    PFIZER PHARMS

    U.S.A
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    Luxepack
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    RLD : Yes

    TE Code :

    HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCURETIC

    Dosage Form : TABLET;ORAL

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

    Approval Date : 1999-12-28

    Application Number : 20125

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    PFIZER PHARMS

    U.S.A
    Luxepack
    Not Confirmed
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    PFIZER PHARMS

    U.S.A
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    RLD : Yes

    TE Code :

    HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCURETIC

    Dosage Form : TABLET;ORAL

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

    Approval Date : 1999-12-28

    Application Number : 20125

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    10

    PFIZER PHARMS

    U.S.A
    Luxepack
    Not Confirmed
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    PFIZER PHARMS

    U.S.A
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    Luxepack
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    RLD : Yes

    TE Code :

    HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCURETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG;EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1999-12-28

    Application Number : 20125

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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