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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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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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    Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.

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    Cefoxitin Sodium

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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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 1Ips Farma Sl

    09 1LABORATORIOS NORMON SA

    10 2Ldp Torlan Laboratories Sa

    11 4Merck & Co

    12 7PHARMOBEDIENT

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    15 2Teva Pharmaceutical Industries

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    01

    B. Braun Medical

    U.S.A
    FNCE
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    Regulatory Info : RX

    Registration Country : USA

    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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    02

    B. Braun Medical

    U.S.A
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    Regulatory Info : RX

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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

    Regulatory Info : RX

    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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    04

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 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    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
    FNCE
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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**

    Packaging :

    Approval Date : 2000-07-03

    Application Number : 65012

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    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 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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    Regulatory Info : RX

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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
    FNCE
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    Hikma Pharmaceuticals

    United Kingdom
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    FNCE
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    Regulatory Info : RX

    Registration Country : USA

    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
    FNCE
    Not Confirmed
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    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

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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
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    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

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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
    FNCE
    Not Confirmed
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    Merck & Co

    U.S.A
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    FNCE
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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
    FNCE
    Not Confirmed
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    Merck & Co

    U.S.A
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    FNCE
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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

    PHARMOBEDIENT

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    PHARMOBEDIENT

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    FNCE
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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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50517

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    PHARMOBEDIENT

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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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    16

    PHARMOBEDIENT

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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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50517

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    PHARMOBEDIENT

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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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    18

    PHARMOBEDIENT

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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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    19

    PHARMOBEDIENT

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    FNCE
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    FNCE
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    20

    PHARMOBEDIENT

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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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