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    List of All Manufacturers & Suppliers of Methylprednisolone Sodium Succinate Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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    Methylprednisolone Sodium Succinate

    ACTIVE PHARMA INGREDIENTS

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    PRICE INFORMATION

    FINISHED DOSAGE FORMULATIONS

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    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

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    01 10ABRAXIS PHARM

    02 4Abbott Laboratories

    03 4Actavis Inc

    04 2Amneal Pharmaceuticals

    05 4Amphastar Pharmaceuticals

    06 4Aurobindo Pharma Limited

    07 6BEDFORD LABS

    08 2Bharat Parenterals Limited

    09 2Chongqing Huapont Pharmaceutical

    10 4ELKINS SINN

    11 1East African (India) Overseas

    12 3Flagship Biotech International Pvt. Ltd

    13 3Fresenius Kabi USA

    14 4Health Biotech

    15 4Hikma Pharmaceuticals

    16 10Hospira, Inc.

    17 3Lisapharma Spa

    18 2Merck & Co

    19 1Modern Laboratories

    20 11Pfizer Inc

    21 3Polifarma

    22 4Quad Pharma

    23 5Sagent Pharmaceuticals

    24 3Teva Pharmaceutical Industries

    25 5Tianjin Tianyao Pharmaceuticals Co., Ltd.

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    01

    BEDFORD LABS

    U.S.A
    AAPS 2024
    Not Confirmed
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    BEDFORD LABS

    U.S.A
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    AAPS 2024
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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 : 2007-02-21

    Application Number : 40641

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    BEDFORD LABS

    U.S.A
    AAPS 2024
    Not Confirmed
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    BEDFORD LABS

    U.S.A
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    AAPS 2024
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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 : 2007-02-21

    Application Number : 40641

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    BEDFORD LABS

    U.S.A
    AAPS 2024
    Not Confirmed
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    BEDFORD LABS

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    AAPS 2024
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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 : 2007-02-21

    Application Number : 40641

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    BEDFORD LABS

    U.S.A
    AAPS 2024
    Not Confirmed
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    BEDFORD LABS

    U.S.A
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    AAPS 2024
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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 40MG BASE/VIAL

    Packaging :

    Approval Date : 2007-02-21

    Application Number : 40662

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    BEDFORD LABS

    U.S.A
    AAPS 2024
    Not Confirmed
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    BEDFORD LABS

    U.S.A
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    AAPS 2024
    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 500MG BASE/VIAL

    Packaging :

    Approval Date : 2007-02-21

    Application Number : 40709

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    BEDFORD LABS

    U.S.A
    AAPS 2024
    Not Confirmed
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    BEDFORD LABS

    U.S.A
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    AAPS 2024
    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 1GM BASE/VIAL

    Packaging :

    Approval Date : 2007-02-21

    Application Number : 40709

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Fresenius Kabi USA

    U.S.A
    AAPS 2024
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    AAPS 2024
    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 : 2004-07-30

    Application Number : 40583

    Regulatory Info : RX

    Registration Country : USA

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    08

    Fresenius Kabi USA

    U.S.A
    AAPS 2024
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    AAPS 2024
    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 : 2004-07-30

    Application Number : 40583

    Regulatory Info : RX

    Registration Country : USA

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    09

    Fresenius Kabi USA

    U.S.A
    AAPS 2024
    Not Confirmed
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    Fresenius Kabi USA

    U.S.A
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    AAPS 2024
    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 1GM BASE/VIAL

    Packaging :

    Approval Date : 2004-08-12

    Application Number : 40612

    Regulatory Info : RX

    Registration Country : USA

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    10

    Hospira, Inc.

    U.S.A
    AAPS 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AAPS 2024
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/VIAL

    Packaging :

    Approval Date : 2005-12-20

    Application Number : 40664

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Hospira, Inc.

    U.S.A
    AAPS 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AAPS 2024
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

    Packaging :

    Approval Date : 2005-12-20

    Application Number : 40665

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
    AAPS 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AAPS 2024
    Not Confirmed
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    METHYLPREDNISOLONE SODIUM SUCCINATE

    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
    AAPS 2024
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    AAPS 2024
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    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : A-METHAPRED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 125MG BASE/VIAL

    Packaging :

    Approval Date : 2008-11-25

    Application Number : 40827

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Pfizer Inc

    U.S.A
    AAPS 2024
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    Regulatory Info : RX

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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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    15

    Pfizer Inc

    U.S.A
    AAPS 2024
    Not Confirmed
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    Pfizer Inc

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    AAPS 2024
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    METHYLPREDNISOLONE SODIUM SUCCINATE

    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

    Registration Country : USA

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    16

    Pfizer Inc

    U.S.A
    AAPS 2024
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    AAPS 2024
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    METHYLPREDNISOLONE SODIUM SUCCINATE

    Brand Name : SOLU-MEDROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11856

    Regulatory Info : RX

    Registration Country : USA

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    17

    Pfizer Inc

    U.S.A
    AAPS 2024
    Not Confirmed
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    Pfizer Inc

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    AAPS 2024
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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

    Regulatory Info : RX

    Registration Country : USA

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    18

    Pfizer Inc

    U.S.A
    AAPS 2024
    Not Confirmed
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    Pfizer Inc

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    AAPS 2024
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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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    19

    Sagent Pharmaceuticals

    U.S.A
    AAPS 2024
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
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    AAPS 2024
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    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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    20

    Sagent Pharmaceuticals

    U.S.A
    AAPS 2024
    Not Confirmed
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    Sagent Pharmaceuticals

    U.S.A
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    AAPS 2024
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    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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