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    Chromic Chloride

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 1Aguettant Laboratory

    02 1B Braun Medical Sa

    03 1Clintec Parenteral

    04 3Fresenius Kabi Espa?a, Sau

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    01

    Aguettant Laboratory

    France
    FNCE
    Not Confirmed
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    Aguettant Laboratory

    France
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    FNCE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Approved

    Registration Country : Sweden

    Iron (II) Gluconate (Anhydrous); Potassium Iodide; Copper Gluconate; Chromium Trichloride Hexahydrate; Manganese Gluconate; Sodium Fluoride; Sodium Molybdate Dihydrate; Sodium Selenite (Anhydrous); Zinc Gluconate (Anhydrous)

    Brand Name : Nutrients

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength :

    Packaging :

    Approval Date : 10/03/2016

    Application Number : 20150501000079

    Regulatory Info : Approved

    Registration Country : Sweden

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    02

    B Braun Medical Sa

    U.S.A
    FNCE
    Not Confirmed
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    B Braun Medical Sa

    U.S.A
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    FNCE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Authorized

    Registration Country : Spain

    Chromium Chloride Hexahydrate; Zinc Chloride; Copper Sulphate Pentahydrate; Manganese Sulphate Monohydrate

    Brand Name : Oligostandard Concentrate For Intravenous Infusion Solution

    Dosage Form : Infusion Solution

    Dosage Strength :

    Packaging :

    Approval Date : 2003-05-19

    Application Number : 65391

    Regulatory Info : Authorized

    Registration Country : Spain

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    03

    Clintec Parenteral

    U.S.A
    FNCE
    Not Confirmed
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    Clintec Parenteral

    U.S.A
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    FNCE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Ammonium Molybdate Tetrahydrate; Ferrous Gluconate Hydrate; Cobalt Gluconate Dihydrate; Copper Gluconate; Chromium Trichloride Hexahydrate; Manganese Gluconate; Sodium Fluoride; Sodium Iodide; Sodium Selenite Anhydrous; Zinc Gluconate Trihydrate

    Brand Name : Decan

    Dosage Form : Concentrate For Solution For Infusion

    Dosage Strength :

    Packaging :

    Approval Date : 26/03/1999

    Application Number : 19990326000151

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    04

    Fresenius Kabi Espa?a, Sau

    Sweden
    FNCE
    Not Confirmed
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    05

    Fresenius Kabi Espa?a, Sau

    Sweden
    FNCE
    Not Confirmed
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    06

    Fresenius Kabi Espa?a, Sau

    Sweden
    FNCE
    Not Confirmed
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