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    METHYLNALTREXONE BROMIDE

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    Dosage Form : SOLUTION;SUBCUTANEOUS

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    METHYLNALTREXONE BROMIDE

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    Methylnaltrexone bromide

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    Methylnaltrexone Bromide

    Brand Name : Relistor

    Dosage Form : Injectable Solution

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    Approval Date : 09-01-2009

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    Methylnaltrexone Bromide

    Brand Name : Relistor

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    Approval Date : 15-07-2008

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    Methylnaltrexone Bromide

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    Approval Date : 15/04/2009

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    METHYLNALTREXONE BROMIDE

    Brand Name : RELISTOR

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 12MG/0.6ML (12MG/0.6ML)

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    Approval Date : 2008-04-24

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    Brand Name : RELISTOR

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 8MG/0.4ML (8MG/0.4ML)

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    Approval Date : 2010-09-27

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    Brand Name : RELISTOR

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    Approval Date : 2010-09-27

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    METHYLNALTREXONE BROMIDE

    Brand Name : RELISTOR

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    Approval Date : 2016-07-19

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    METHYLNALTREXONE BROMIDE

    Brand Name : METHYLNALTREXONE BROMIDE

    Dosage Form : SOLUTION;SUBCUTANEOUS

    Dosage Strength : 12MG/0.6ML (12MG/0.6ML)

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    Approval Date : 2025-05-28

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    US GENERICS, STERILES

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    METHYLNALTREXONE BROMIDE

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    Relistor

    Brand Name : Relistor

    Dosage Form : Metilnaltrexone 12Mg 7 Joined The Parenteral Use

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    Regulatory Info : Prescription

    Registration Country : Denmark

    Methylnaltrexone Bromide

    Brand Name : Relistor

    Dosage Form : Injection Solution

    Dosage Strength : 12mg/0.6ml

    Packaging :

    Approval Date : 02-07-2008

    Application Number : 28104188907

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    Registration Country : Denmark

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