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    Approved Drug Products containing Pralidoxime Methyl Sulphate listed in the FDA Orange Book. Original Data : FDA Website

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    Evonik

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    Fishfa Biogenics: Renowned Manufacturer, & Exporter of Tacrolimus & Mupirocin API.

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    xyz-pharma-m-2024-10-07

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    xyz-pharma-m-2024-10-07

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    Pralidoxime Methyl Sulphate

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

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    REF. STANDARDS & IMPURITIES

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    01 2BAXTER HLTHCARE CORP

    02 1MERIDIAN MEDCL TECHN

    03 1MMT

    04 1QUAD PHARMS

    05 1US ARMY

    06 1WYETH AYERST

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    01

    BAXTER HLTHCARE CORP

    U.S.A
    World Vaccine Congress
    Not Confirmed
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    BAXTER HLTHCARE CORP

    U.S.A
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    World Vaccine Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    PRALIDOXIME CHLORIDE

    Brand Name : PROTOPAM CHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1GM/VIAL

    Approval Date : 1982-01-01

    Application Number : 14134

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    BAXTER HLTHCARE CORP

    U.S.A
    World Vaccine Congress
    Not Confirmed
    arrow

    BAXTER HLTHCARE CORP

    U.S.A
    arrow
    World Vaccine Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    PRALIDOXIME CHLORIDE

    Brand Name : PRALIDOXIME CHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 300MG/ML

    Approval Date : 1982-12-13

    Application Number : 18799

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    MMT

    U.S.A
    World Vaccine Congress
    Not Confirmed
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    MMT

    U.S.A
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    World Vaccine Congress
    Not Confirmed
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    RLD : Yes

    TE Code :

    ATROPINE; PRALIDOXIME CHLORIDE

    Brand Name : DUODOTE

    Dosage Form : INJECTABLE;INTRAMUSCULAR

    Dosage Strength : 2.1MG/0.7ML;600MG/2ML

    Approval Date : 2006-09-28

    Application Number : 21983

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    MERIDIAN MEDCL TECHN

    U.S.A
    World Vaccine Congress
    Not Confirmed
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    MERIDIAN MEDCL TECHN

    U.S.A
    arrow
    World Vaccine Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    PRALIDOXIME CHLORIDE

    Brand Name : PRALIDOXIME CHLORIDE (AUTOINJECTOR)

    Dosage Form : SOLUTION;INTRAMUSCULAR

    Dosage Strength : 600MG/2ML (300MG/ML)

    Approval Date : 1983-04-26

    Application Number : 18986

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    05

    QUAD PHARMS

    South Africa
    World Vaccine Congress
    Not Confirmed
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    QUAD PHARMS

    South Africa
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    World Vaccine Congress
    Not Confirmed
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    RLD :

    TE Code :

    PRALIDOXIME CHLORIDE

    Brand Name : PRALIDOXIME CHLORIDE

    Dosage Form : Injectable; Injection

    Dosage Strength : 1GM/VIAL

    Approval Date :

    Application Number : 72224

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    06

    WYETH AYERST

    U.S.A
    World Vaccine Congress
    Not Confirmed
    arrow

    WYETH AYERST

    U.S.A
    arrow
    World Vaccine Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    PRALIDOXIME CHLORIDE

    Brand Name : PROTOPAM CHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 500MG

    Approval Date : 1982-01-01

    Application Number : 14122

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    07

    US ARMY

    Country
    World Vaccine Congress
    Not Confirmed
    arrow

    US ARMY

    Country
    arrow
    World Vaccine Congress
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    ATROPINE; PRALIDOXIME CHLORIDE

    Brand Name : ATNAA

    Dosage Form : INJECTABLE;INTRAMUSCULAR

    Dosage Strength : 2.1MG/0.7ML;600MG/2ML

    Approval Date : 2002-01-17

    Application Number : 21175

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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