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    Methyldopate Hydrochloride

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    REF. STANDARDS & IMPURITIES

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    01 1ABRAXIS PHARM

    02 1AM REGENT

    03 1BAXTER HLTHCARE

    04 4HOSPIRA

    05 1MARSAM PHARMS LLC

    06 1MERCK

    07 1QUAD PHARMS

    08 1SMITH AND NEPHEW

    09 1TEVA PARENTERAL

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    01

    ABRAXIS PHARM

    U.S.A
    BioAsia
    Not Confirmed
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    ABRAXIS PHARM

    U.S.A
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    RLD : No

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : METHYLDOPATE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1986-06-03

    Application Number : 70652

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    AM REGENT

    U.S.A
    BioAsia
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    AM REGENT

    U.S.A
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    RLD : No

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : METHYLDOPATE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1987-10-02

    Application Number : 71279

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    BAXTER HLTHCARE

    U.S.A
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    BAXTER HLTHCARE

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    RLD : No

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : METHYLDOPATE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1986-07-01

    Application Number : 70291

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    HOSPIRA

    U.S.A
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    HOSPIRA

    U.S.A
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    RLD : No

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : METHYLDOPATE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1987-06-19

    Application Number : 70691

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    HOSPIRA

    U.S.A
    BioAsia
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    HOSPIRA

    U.S.A
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    RLD : No

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : METHYLDOPATE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1987-06-15

    Application Number : 70698

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    HOSPIRA

    U.S.A
    BioAsia
    Not Confirmed
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    HOSPIRA

    U.S.A
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    BioAsia
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    RLD : No

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : METHYLDOPATE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1987-06-15

    Application Number : 70699

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    HOSPIRA

    U.S.A
    BioAsia
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    HOSPIRA

    U.S.A
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    RLD : No

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : METHYLDOPATE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1987-06-19

    Application Number : 70849

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    MERCK

    U.S.A
    BioAsia
    Not Confirmed
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    MERCK

    U.S.A
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    BioAsia
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    RLD : Yes

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : ALDOMET

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 13401

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    QUAD PHARMS

    South Africa
    BioAsia
    Not Confirmed
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    QUAD PHARMS

    South Africa
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    BioAsia
    Not Confirmed
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    RLD :

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : METHYLDOPATE HCL

    Dosage Form : Injectable; Injection

    Dosage Strength : 50MG/ML

    Approval Date :

    Application Number : 71024

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    10

    SMITH AND NEPHEW

    Canada
    BioAsia
    Not Confirmed
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    SMITH AND NEPHEW

    Canada
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    BioAsia
    Not Confirmed
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    RLD : No

    TE Code :

    METHYLDOPATE HYDROCHLORIDE

    Brand Name : METHYLDOPATE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 50MG/ML

    Approval Date : 1987-01-02

    Application Number : 70841

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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