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    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    Cefoxitin Sodium

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    Dosage Strength : EQ 2GM BASE/VIAL

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    Brand Name : CEFOXITIN

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    Dosage Strength : EQ 10GM BASE/VIAL

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    Approval Date : 2000-07-03

    Application Number : 65011

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    Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    Fresenius Kabi USA

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    Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    Hikma Pharmaceuticals

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    Brand Name : CEFOXITIN

    Dosage Form : INJECTABLE;INJECTION

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    Approval Date : 2000-09-11

    Application Number : 65050

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    Hikma Pharmaceuticals

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    Brand Name : CEFOXITIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2000-09-11

    Application Number : 65051

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    Hikma Pharmaceuticals

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    Brand Name : CEFOXITIN

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    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 2000-09-11

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    Hikma Pharmaceuticals

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    Approval Date : 2010-03-12

    Application Number : 65238

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    Approval Date : 2010-03-12

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    Approval Date : 2010-03-02

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    Hospira, Inc.

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    Brand Name : CEFOXITIN

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    Approval Date : 2006-02-13

    Application Number : 65312

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    Hospira, Inc.

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    Brand Name : CEFOXITIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 2006-01-23

    Application Number : 65313

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    Hospira, Inc.

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    Brand Name : CEFOXITIN

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    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 2006-01-23

    Application Number : 65313

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    Merck & Co

    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**

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    Approval Date : 1984-09-20

    Application Number : 50581

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    Merck & Co

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    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**

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    Approval Date : 1984-09-20

    Application Number : 50581

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    Merck & Co

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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**

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    Approval Date : 1984-09-20

    Application Number : 50581

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    Merck & Co

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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**

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    Approval Date : 1984-09-20

    Application Number : 50581

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

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    Approval Date : 1982-01-01

    Application Number : 50517

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    Registration Country : USA

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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**

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    Approval Date : 1982-01-01

    Application Number : 50517

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

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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**

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    Approval Date : 1982-01-01

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    Registration Country : USA

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    Regulatory Info : DISCN

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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

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    Registration Country : USA

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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

    Packaging :

    Approval Date : 1987-01-08

    Application Number : 62757

    Regulatory Info : DISCN

    Registration Country : USA

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    29

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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

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    Registration Country : USA

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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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