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    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 2005-12-20

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    Approval Date : 2008-11-25

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    Approval Date : 1982-01-01

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    Approval Date : 1982-01-01

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    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 1982-01-01

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    Dosage Strength : EQ 125MG BASE/VIAL

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    Approval Date : 1982-01-01

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    Dosage Strength : EQ 40MG BASE/VIAL

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    Approval Date : 1982-01-01

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    Regulatory Info : RX

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : SOLU-MEDROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1985-02-27

    Application Number : 11856

    Regulatory Info : RX

    Registration Country : USA

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    23

    Sagent Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/VIAL

    Packaging :

    Approval Date : 2011-07-18

    Application Number : 40888

    Regulatory Info : RX

    Registration Country : USA

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    24

    Sagent Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Sagent Pharmaceuticals

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : RX

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

    Packaging :

    Approval Date : 2011-07-18

    Application Number : 40888

    Regulatory Info : RX

    Registration Country : USA

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    25

    Sagent Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : RX

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 2011-07-18

    Application Number : 40888

    Regulatory Info : RX

    Registration Country : USA

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    26

    Sagent Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : RX

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 2011-07-18

    Application Number : 40888

    Regulatory Info : RX

    Registration Country : USA

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    27

    Sagent Pharmaceuticals

    U.S.A
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Sagent Pharmaceuticals

    U.S.A
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : RX

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 2011-07-18

    Application Number : 40888

    Regulatory Info : RX

    Registration Country : USA

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    28

    Teva Pharmaceutical Industries

    Israel
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

    Packaging :

    Approval Date : 1992-11-30

    Application Number : 81266

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    Teva Pharmaceutical Industries

    Israel
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1992-11-30

    Application Number : 81267

    Regulatory Info : DISCN

    Registration Country : USA

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    30

    Teva Pharmaceutical Industries

    Israel
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    Teva Pharmaceutical Industries

    Israel
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : DISCN

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1992-11-30

    Application Number : 81268

    Regulatory Info : DISCN

    Registration Country : USA

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