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    Methylprednisolone Sodium Succinate

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    PFIZER CANADA ULC

    U.S.A
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    Not Confirmed
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    PFIZER CANADA ULC

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    Regulatory Info : Prescription

    Registration Country : Canada

    METHYLPREDNISOLONE (METHYLPREDNISOLONE SODIUM SUCCINATE)

    Brand Name : SOLU-MEDROL

    Dosage Form : KIT

    Dosage Strength : 1G/VIAL

    Packaging : 1X8ML

    Approval Date :

    Application Number : 36137

    Regulatory Info : Prescription

    Registration Country : Canada

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    PFIZER CANADA ULC

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    PFIZER CANADA ULC

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    METHYLPREDNISOLONE (METHYLPREDNISOLONE SODIUM SUCCINATE)

    Brand Name : SOLU-MEDROL

    Dosage Form : KIT

    Dosage Strength : 500MG/VIAL

    Packaging : 5X4ML

    Approval Date :

    Application Number : 30678

    Regulatory Info : Prescription

    Registration Country : Canada

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    PFIZER CANADA ULC

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    METHYLPREDNISOLONE (METHYLPREDNISOLONE SODIUM SUCCINATE)

    Brand Name : SOLU-MEDROL

    Dosage Form : KIT

    Dosage Strength : 40MG/VIAL

    Packaging : 10X1ML

    Approval Date :

    Application Number : 2367947

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    Registration Country : Canada

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    04

    PFIZER CANADA ULC

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    METHYLPREDNISOLONE (METHYLPREDNISOLONE SODIUM SUCCINATE)

    Brand Name : SOLU-MEDROL

    Dosage Form : KIT

    Dosage Strength : 125MG/VIAL

    Packaging : 10X2ML

    Approval Date :

    Application Number : 2367955

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    Registration Country : Canada

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    05

    PFIZER CANADA ULC

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    METHYLPREDNISOLONE (METHYLPREDNISOLONE SODIUM SUCCINATE)

    Brand Name : SOLU-MEDROL

    Dosage Form : KIT

    Dosage Strength : 500MG/VIAL

    Packaging : 5X4ML

    Approval Date :

    Application Number : 2367963

    Regulatory Info : Prescription

    Registration Country : Canada

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    06

    PFIZER CANADA ULC

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    PFIZER CANADA ULC

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    Pharma, Lab & Chemical Expo
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    Regulatory Info : Prescription

    Registration Country : Canada

    METHYLPREDNISOLONE (METHYLPREDNISOLONE SODIUM SUCCINATE)

    Brand Name : SOLU-MEDROL

    Dosage Form : KIT

    Dosage Strength : 1G/VIAL

    Packaging : 1X8ML

    Approval Date :

    Application Number : 2367971

    Regulatory Info : Prescription

    Registration Country : Canada

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