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    Amiloride Hydrochloride

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

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    01 1BARR

    02 2CHARTWELL RX

    03 1ENDO OPERATIONS

    04 1MERCK

    05 1PADAGIS US

    06 1PAR PHARM

    07 1RISING

    08 1SIGMAPHARM LABS LLC

    09 1TEVA

    10 1WATSON LABS

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    01

    WATSON LABS

    Ireland
    American Pharma Summit
    Not Confirmed
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    WATSON LABS

    Ireland
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    RLD : No

    TE Code :

    AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG ANHYDROUS;50MG

    Approval Date : 1991-07-19

    Application Number : 73334

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    BARR

    U.S.A
    American Pharma Summit
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    BARR

    U.S.A
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    RLD : No

    TE Code : AB

    AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG ANHYDROUS;50MG

    Approval Date : 1988-05-10

    Application Number : 71111

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    CHARTWELL RX

    U.S.A
    American Pharma Summit
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    CHARTWELL RX

    U.S.A
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    RLD : No

    TE Code :

    AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG ANHYDROUS;50MG

    Approval Date : 1991-11-27

    Application Number : 73357

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    MERCK

    U.S.A
    American Pharma Summit
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    MERCK

    U.S.A
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    RLD : Yes

    TE Code :

    AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : MODURETIC 5-50

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG ANHYDROUS;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 18201

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    05

    PADAGIS US

    Israel
    American Pharma Summit
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    PADAGIS US

    Israel
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    RLD : Yes

    TE Code : AB

    AMILORIDE HYDROCHLORIDE

    Brand Name : MIDAMOR

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date : 1982-01-01

    Application Number : 18200

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    06

    PAR PHARM

    U.S.A
    American Pharma Summit
    Not Confirmed
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    PAR PHARM

    U.S.A
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    RLD : No

    TE Code :

    AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : HYDRO-RIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG ANHYDROUS;50MG

    Approval Date : 1990-12-25

    Application Number : 70347

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    RISING

    U.S.A
    American Pharma Summit
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    RISING

    U.S.A
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    RLD : No

    TE Code : AB

    AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG ANHYDROUS;50MG

    Approval Date : 1991-10-31

    Application Number : 73209

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    SIGMAPHARM LABS LLC

    U.S.A
    American Pharma Summit
    Not Confirmed
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    SIGMAPHARM LABS LLC

    U.S.A
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    American Pharma Summit
    Not Confirmed
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    RLD : No

    TE Code : AB

    AMILORIDE HYDROCHLORIDE

    Brand Name : AMILORIDE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date : 2009-01-30

    Application Number : 79133

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    TEVA

    Israel
    American Pharma Summit
    Not Confirmed
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    TEVA

    Israel
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    Not Confirmed
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    RLD : No

    TE Code :

    AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

    Brand Name : AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG ANHYDROUS;50MG

    Approval Date : 1988-04-17

    Application Number : 70795

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    ENDO OPERATIONS

    Country
    American Pharma Summit
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    RLD : No

    TE Code : AB

    AMILORIDE HYDROCHLORIDE

    Brand Name : AMILORIDE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Approval Date : 1986-01-22

    Application Number : 70346

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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