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    01

    Strides Pharma Science

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    Regulatory Info : Generic

    Registration Country : South Africa

    Hydrocortisone Sodium Succinate USP equivalent to Hydrocortisone

    Brand Name : CORTAJECT 100 mg

    Dosage Form : INJ

    Dosage Strength : 100mg /5ml

    Packaging : 1X1mg

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    Regulatory Info : Generic

    Registration Country : South Africa

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    02

    Abbott Laboratories

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    Regulatory Info : DISCN

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    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : A-HYDROCORT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 100MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85928

    Regulatory Info : DISCN

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    03

    Actavis Inc

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    Regulatory Info : DISCN

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    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : HYDROCORTISONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 250MG BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 84737

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    04

    Actavis Inc

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    Regulatory Info : DISCN

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    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : HYDROCORTISONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 100MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 84737

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Actavis Inc

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    Regulatory Info : DISCN

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    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : HYDROCORTISONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 100MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 84738

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Actavis Inc

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    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : HYDROCORTISONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 84747

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Actavis Inc

    Ireland
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    Actavis Inc

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    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : HYDROCORTISONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 1982-01-01

    Application Number : 84748

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    Registration Country : USA

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    08

    Amphastar Pharmaceuticals

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    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : HYDROCORTISONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 100MG BASE/VIAL

    Packaging :

    Approval Date : 1982-03-19

    Application Number : 87532

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Baxter Healthcare Corporation

    U.S.A
    ASCO GU
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    ASCO GU
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : HYDROCORTISONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 100MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86619

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Baxter Healthcare Corporation

    U.S.A
    ASCO GU
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
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    ASCO GU
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : HYDROCORTISONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 250MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 87567

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Baxter Healthcare Corporation

    U.S.A
    ASCO GU
    Not Confirmed
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    Baxter Healthcare Corporation

    U.S.A
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    ASCO GU
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : HYDROCORTISONE SODIUM SUCCINATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 87568

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
    ASCO GU
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASCO GU
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : A-HYDROCORT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 100MG BASE/VIAL

    Packaging :

    Approval Date : 2006-04-06

    Application Number : 40666

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Hospira, Inc.

    U.S.A
    ASCO GU
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASCO GU
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : A-HYDROCORT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 100MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85929

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Hospira, Inc.

    U.S.A
    ASCO GU
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASCO GU
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : A-HYDROCORT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 250MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85930

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Hospira, Inc.

    U.S.A
    ASCO GU
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASCO GU
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : A-HYDROCORT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85931

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Hospira, Inc.

    U.S.A
    ASCO GU
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    ASCO GU
    Not Confirmed
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    Regulatory Info : DISCN

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    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : A-HYDROCORT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85932

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Pfizer Inc

    U.S.A
    ASCO GU
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    ASCO GU
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    Regulatory Info : RX

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : SOLU-CORTEF

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 100MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 9866

    Regulatory Info : RX

    Registration Country : USA

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    18

    Pfizer Inc

    U.S.A
    ASCO GU
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    Pfizer Inc

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    ASCO GU
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    Regulatory Info : RX

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    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : SOLU-CORTEF

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 250MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 9866

    Regulatory Info : RX

    Registration Country : USA

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    19

    Pfizer Inc

    U.S.A
    ASCO GU
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    ASCO GU
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : SOLU-CORTEF

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 9866

    Regulatory Info : RX

    Registration Country : USA

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    20

    Pfizer Inc

    U.S.A
    ASCO GU
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    ASCO GU
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    Regulatory Info : RX

    Registration Country : USA

    HYDROCORTISONE SODIUM SUCCINATE

    Brand Name : SOLU-CORTEF

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 9866

    Regulatory Info : RX

    Registration Country : USA

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