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    CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

    ACTIVE PHARMA INGREDIENTS

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    01 2ACS DOBFAR SPA

    02 2Apotex Inc

    03 4Aurogen South Africa (Pty) Ltd

    04 2B. Braun Medical

    05 2Baxter Healthcare Corporation

    06 2Belco Pharma

    07 3Chartwell Pharmaceuticals llc

    08 1Doctor's Life Sciences

    09 4Fresenius SE & Co. KGaA

    10 3Hikma Pharmaceuticals

    11 8Hospira, Inc.

    12 2MIP Pharma

    13 3Qilu Antibiotics Pharmaceutical Co., Ltd.

    14 2Sagent Pharmaceuticals

    15 1Samson Medical Technologies

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    01

    ACS DOBFAR SPA

    Italy
    Pharmex
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    ACS DOBFAR SPA

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    Regulatory Info : RX

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 2008-03-20

    Application Number : 65441

    Regulatory Info : RX

    Registration Country : USA

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    02

    ACS DOBFAR SPA

    Italy
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 2008-03-20

    Application Number : 65441

    Regulatory Info : RX

    Registration Country : USA

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    03

    B. Braun Medical

    U.S.A
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 2010-05-06

    Application Number : 50821

    Regulatory Info : RX

    Registration Country : USA

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    04

    B. Braun Medical

    U.S.A
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 2010-05-06

    Application Number : 50821

    Regulatory Info : RX

    Registration Country : USA

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    05

    Baxter Healthcare Corporation

    U.S.A
    Pharmex
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/50ML (EQ 20MG BASE/ML)

    Packaging :

    Approval Date : 2008-08-05

    Application Number : 50817

    Regulatory Info : RX

    Registration Country : USA

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    06

    Baxter Healthcare Corporation

    U.S.A
    Pharmex
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/100ML (EQ 20MG BASE/ML)

    Packaging :

    Approval Date : 2008-08-05

    Application Number : 50817

    Regulatory Info : RX

    Registration Country : USA

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    07

    Chartwell Pharmaceuticals llc

    U.S.A
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    Chartwell Pharmaceuticals llc

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 2010-12-21

    Application Number : 90291

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Chartwell Pharmaceuticals llc

    U.S.A
    Pharmex
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    Regulatory Info : DISCN

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 2010-12-21

    Application Number : 90291

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Chartwell Pharmaceuticals llc

    U.S.A
    Pharmex
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    U.S.A
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    Regulatory Info : DISCN

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 2010-12-21

    Application Number : 90291

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Hospira, Inc.

    U.S.A
    Pharmex
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    Pharmex
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    Regulatory Info : DISCN

    Registration Country : USA

    CEFEPIME HYDROCHLORIDE

    Brand Name : MAXIPIME

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1996-01-18

    Application Number : 50679

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Hospira, Inc.

    U.S.A
    Pharmex
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    Hospira, Inc.

    U.S.A
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    Pharmex
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    Regulatory Info : DISCN

    Registration Country : USA

    CEFEPIME HYDROCHLORIDE

    Brand Name : MAXIPIME

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1996-01-18

    Application Number : 50679

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
    Pharmex
    Not Confirmed
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    Hospira, Inc.

    U.S.A
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    Pharmex
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    Regulatory Info : DISCN

    Registration Country : USA

    CEFEPIME HYDROCHLORIDE

    Brand Name : MAXIPIME

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1996-01-18

    Application Number : 50679

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Hospira, Inc.

    U.S.A
    Pharmex
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    Hospira, Inc.

    U.S.A
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    Regulatory Info : DISCN

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 2007-06-18

    Application Number : 65369

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Hospira, Inc.

    U.S.A
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 2007-06-18

    Application Number : 65369

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Hospira, Inc.

    U.S.A
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 2007-06-18

    Application Number : 65369

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Hospira, Inc.

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 2012-07-30

    Application Number : 202268

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Hospira, Inc.

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 2012-07-30

    Application Number : 202268

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Qilu Antibiotics Pharmaceutical Co....

    China
    Pharmex
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    Qilu Antibiotics Pharmaceutical Co....

    China
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 2016-02-01

    Application Number : 203704

    Regulatory Info : RX

    Registration Country : USA

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    19

    Sagent Pharmaceuticals

    U.S.A
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    Sagent Pharmaceuticals

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 2017-01-04

    Application Number : 91048

    Regulatory Info : RX

    Registration Country : USA

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    20

    Sagent Pharmaceuticals

    U.S.A
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 2017-01-04

    Application Number : 91048

    Regulatory Info : RX

    Registration Country : USA

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