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    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

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    Approval Date : 2007-02-21

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    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

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    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/VIAL

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    Approval Date : 2007-02-21

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    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 2007-02-21

    Application Number : 40709

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    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2007-02-21

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    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/VIAL

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    Approval Date : 2004-07-30

    Application Number : 40583

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    Fresenius Kabi USA

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    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

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    Approval Date : 2004-07-30

    Application Number : 40583

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    09

    Fresenius Kabi USA

    U.S.A
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    Brand Name : METHYLPREDNISOLONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2004-08-12

    Application Number : 40612

    Regulatory Info : RX

    Registration Country : USA

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    10

    Hospira, Inc.

    U.S.A
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    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/VIAL

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    Approval Date : 2005-12-20

    Application Number : 40664

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Hospira, Inc.

    U.S.A
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    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

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    Approval Date : 2005-12-20

    Application Number : 40665

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
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    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/VIAL

    Packaging :

    Approval Date : 2008-11-25

    Application Number : 40793

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Hospira, Inc.

    U.S.A
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    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

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    Approval Date : 2008-11-25

    Application Number : 40827

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Hospira, Inc.

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    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85852

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Hospira, Inc.

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    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85853

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Hospira, Inc.

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    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85854

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Hospira, Inc.

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    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 85855

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Pfizer Inc

    U.S.A
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    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : SOLU-MEDROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11856

    Regulatory Info : RX

    Registration Country : USA

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    19

    Pfizer Inc

    U.S.A
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    Brand Name : SOLU-MEDROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11856

    Regulatory Info : RX

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    20

    Pfizer Inc

    U.S.A
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    Brand Name : SOLU-MEDROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 11856

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    Pfizer Inc

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    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : SOLU-MEDROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11856

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    Pfizer Inc

    U.S.A
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    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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    Sagent Pharmaceuticals

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    Sagent Pharmaceuticals

    U.S.A
    arrow
    ELCC
    Not Confirmed
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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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    Sagent Pharmaceuticals

    U.S.A
    ELCC
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
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    ELCC
    Not Confirmed
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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
    ELCC
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
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    ELCC
    Not Confirmed
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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
    ELCC
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
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    ELCC
    Not Confirmed
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    • 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 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
    ELCC
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
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    ELCC
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

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    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
    ELCC
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    ELCC
    Not Confirmed
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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
    ELCC
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    ELCC
    Not Confirmed
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    Regulatory Info : DISCN

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    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
    ELCC
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    ELCC
    Not Confirmed
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    • EDQM
    • WHO-GMP
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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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