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    MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

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    01 6ACS DOBFAR SPA

    02 2B. Braun Medical

    03 1Cathay Drug Company

    04 3Fresenius Kabi USA

    05 3Hainan Haiyao

    06 6Hikma Pharmaceuticals

    07 3Hospira, Inc.

    08 4Merck & Co

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    01

    B. Braun Medical

    U.S.A
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    CEFOXITIN SODIUM

    Brand Name : CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2006-03-10

    Application Number : 65214

    Regulatory Info : RX

    Registration Country : USA

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    U.S.A
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    CEFOXITIN SODIUM

    Brand Name : CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 2006-03-10

    Application Number : 65214

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    Registration Country : USA

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    03

    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : DISCN

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    CEFOXITIN SODIUM

    Brand Name : CEFOXITIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10GM BASE/VIAL

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    Approval Date : 2000-07-03

    Application Number : 65011

    Regulatory Info : DISCN

    Registration Country : USA

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    Fresenius Kabi USA

    U.S.A
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    CEFOXITIN SODIUM

    Brand Name : CEFOXITIN

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    Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2000-07-03

    Application Number : 65012

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : DISCN

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    CEFOXITIN SODIUM

    Brand Name : CEFOXITIN

    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**

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    Approval Date : 2000-07-03

    Application Number : 65012

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Hikma Pharmaceuticals

    United Kingdom
    AACR Annual meeting
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    CEFOXITIN SODIUM

    Brand Name : CEFOXITIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10GM BASE/VIAL

    Packaging :

    Approval Date : 2000-09-11

    Application Number : 65050

    Regulatory Info : RX

    Registration Country : USA

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    07

    Hikma Pharmaceuticals

    United Kingdom
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    CEFOXITIN SODIUM

    Brand Name : CEFOXITIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 2000-09-11

    Application Number : 65051

    Regulatory Info : RX

    Registration Country : USA

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    08

    Hikma Pharmaceuticals

    United Kingdom
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    Regulatory Info : RX

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    CEFOXITIN SODIUM

    Brand Name : CEFOXITIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 2000-09-11

    Application Number : 65051

    Regulatory Info : RX

    Registration Country : USA

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    09

    Hikma Pharmaceuticals

    United Kingdom
    AACR Annual meeting
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    United Kingdom
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    CEFOXITIN SODIUM

    Brand Name : CEFOXITIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 2010-03-12

    Application Number : 65238

    Regulatory Info : RX

    Registration Country : USA

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    10

    Merck & Co

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    U.S.A
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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-09-20

    Application Number : 50581

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Merck & Co

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    U.S.A
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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-09-20

    Application Number : 50581

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Merck & Co

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    U.S.A
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    AACR Annual meeting
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    Regulatory Info : DISCN

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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-09-20

    Application Number : 50581

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Merck & Co

    U.S.A
    AACR Annual meeting
    Not Confirmed
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    U.S.A
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    AACR Annual meeting
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    Regulatory Info : DISCN

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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1984-09-20

    Application Number : 50581

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    NORVIUM BIOSCIENCE

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    AACR Annual meeting
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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN

    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 : 1982-01-01

    Application Number : 50517

    Regulatory Info : DISCN

    Registration Country : USA

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    NORVIUM BIOSCIENCE

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    Regulatory Info : DISCN

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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN

    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 : 1982-01-01

    Application Number : 50517

    Regulatory Info : DISCN

    Registration Country : USA

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    NORVIUM BIOSCIENCE

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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50517

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    NORVIUM BIOSCIENCE

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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1987-01-08

    Application Number : 62757

    Regulatory Info : DISCN

    Registration Country : USA

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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1987-01-08

    Application Number : 62757

    Regulatory Info : DISCN

    Registration Country : USA

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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/ML

    Packaging :

    Approval Date : 1993-01-25

    Application Number : 63182

    Regulatory Info : DISCN

    Registration Country : USA

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    NORVIUM BIOSCIENCE

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    CEFOXITIN SODIUM

    Brand Name : MEFOXIN IN PLASTIC CONTAINER

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 40MG BASE/ML

    Packaging :

    Approval Date : 1993-01-25

    Application Number : 63182

    Regulatory Info : DISCN

    Registration Country : USA

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