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    manganese chloride, hexahydrate

    ACTIVE PHARMA INGREDIENTS

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    02 1Hospira, Inc.

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    01

    Fresenius SE & Co. KGaA

    Germany
    Medlab Asia & Asia Health
    Not Confirmed
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    Fresenius SE & Co. KGaA

    Germany
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    Medlab Asia & Asia Health
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    Regulatory Info : Originator

    Registration Country : South Africa

    Manganese Chloride

    Brand Name : Additrace

    Dosage Form : INF

    Dosage Strength : 99mcg

    Packaging : 10X20mcg/ml

    Approval Date :

    Application Number :

    Regulatory Info : Originator

    Registration Country : South Africa

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    Fresenius SE & Co. KGaA

    Germany
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    Fresenius SE & Co. KGaA

    Germany
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    Regulatory Info : Originator

    Registration Country : South Africa

    Manganese Chloride

    Brand Name : Additrace

    Dosage Form : INF

    Dosage Strength : 99mcg

    Packaging : 10X1mcg/ml

    Approval Date :

    Application Number :

    Regulatory Info : Originator

    Registration Country : South Africa

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    03

    Fresenius SE & Co. KGaA

    Germany
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    Regulatory Info : Originator

    Registration Country : South Africa

    Manganese Chloride

    Brand Name : Peditrace

    Dosage Form : SOL

    Dosage Strength : 100g

    Packaging : 10X10mcg

    Approval Date :

    Application Number :

    Regulatory Info : Originator

    Registration Country : South Africa

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    Fresenius SE & Co. KGaA

    Germany
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    Regulatory Info : Originator

    Registration Country : South Africa

    Manganese Chloride

    Brand Name : Peditrace

    Dosage Form : SOL

    Dosage Strength : 521mcg

    Packaging : 10X1mcg

    Approval Date :

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    Regulatory Info : Originator

    Registration Country : South Africa

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    Hospira, Inc.

    U.S.A
    Medlab Asia & Asia Health
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    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    MANGANESE CHLORIDE

    Brand Name : MANGANESE CHLORIDE IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 0.1MG MANGANESE/ML

    Packaging :

    Approval Date : 1986-06-26

    Application Number : 18962

    Regulatory Info : RX

    Registration Country : USA

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