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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Kewpie is your partner for Sodium Hyaluronate & Hyaluronic Acid// CEP, USDMF, KDMF & JDMF registered.

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    Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.

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    Cefoxitin Sodium

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    Approval Date : 2006-01-23

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

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    Dosage Strength : EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    Dosage Strength : EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    Brand Name : MEFOXIN IN DEXTROSE 5% IN PLASTIC CONTAINER

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    Dosage Strength : EQ 20MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    Merck & Co

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    Dosage Strength : EQ 40MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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

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    NORVIUM BIOSCIENCE

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    Regulatory Info : DISCN

    Registration Country : USA

    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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    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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    Regulatory Info : DISCN

    Registration Country : USA

    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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    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

    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 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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    Regulatory Info : DISCN

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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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    Regulatory Info : DISCN

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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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