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    CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

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    05 2Baxter Healthcare Corporation

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    07 3Chartwell Pharmaceuticals llc

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    ACS DOBFAR SPA

    Italy
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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2008-03-20

    Application Number : 65441

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    Brand Name : CEFEPIME HYDROCHLORIDE

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    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 2008-03-20

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    03

    B. Braun Medical

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2010-05-06

    Application Number : 50821

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    Registration Country : USA

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    B. Braun Medical

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    CEFEPIME HYDROCHLORIDE

    Brand Name : CEFEPIME AND DEXTROSE IN DUPLEX CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 2010-05-06

    Application Number : 50821

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    05

    Baxter Healthcare Corporation

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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)

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    Approval Date : 2008-08-05

    Application Number : 50817

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    Baxter Healthcare Corporation

    U.S.A
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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)

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    Approval Date : 2008-08-05

    Application Number : 50817

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    Registration Country : USA

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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

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    Approval Date : 2010-12-21

    Application Number : 90291

    Regulatory Info : DISCN

    Registration Country : USA

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    Chartwell Pharmaceuticals llc

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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
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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 : 2010-12-21

    Application Number : 90291

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Hospira, Inc.

    U.S.A
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    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**

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    Approval Date : 1996-01-18

    Application Number : 50679

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Hospira, Inc.

    U.S.A
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    Regulatory Info : DISCN

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    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
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    Regulatory Info : DISCN

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    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
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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.

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    Brand Name : CEFEPIME HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2007-06-18

    Application Number : 65369

    Regulatory Info : DISCN

    Registration Country : USA

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    Hospira, Inc.

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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 : 2007-06-18

    Application Number : 65369

    Regulatory Info : DISCN

    Registration Country : USA

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    Hospira, Inc.

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    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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    Hospira, Inc.

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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 : 2012-07-30

    Application Number : 202268

    Regulatory Info : DISCN

    Registration Country : USA

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    Qilu Antibiotics Pharmaceutical Co....

    China
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    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

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    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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    Sagent Pharmaceuticals

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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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