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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.

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    Cephapirin Sodium

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    $ API Ref.Price (USD/KG) : 408,600Xls

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    01 5ABRAXIS PHARM

    02 1Boehringer Ingelheim GmbH

    03 14Bristol Myers Squibb

    04 4Hikma Pharmaceuticals

    05 1Qilu Animal Health Products

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    01

    ABRAXIS PHARM

    U.S.A
    ICHH-25
    Not Confirmed
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    ABRAXIS PHARM

    U.S.A
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    ICHH-25
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEPHAPIRIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

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    Approval Date : 1986-11-17

    Application Number : 62723

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    ABRAXIS PHARM

    U.S.A
    ICHH-25
    Not Confirmed
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    ABRAXIS PHARM

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEPHAPIRIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

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    Approval Date : 1986-11-17

    Application Number : 62723

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    ABRAXIS PHARM

    U.S.A
    ICHH-25
    Not Confirmed
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    ABRAXIS PHARM

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEPHAPIRIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

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    Approval Date : 1986-11-17

    Application Number : 62723

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    ABRAXIS PHARM

    U.S.A
    ICHH-25
    Not Confirmed
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEPHAPIRIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/VIAL

    Packaging :

    Approval Date : 1986-11-17

    Application Number : 62723

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    ABRAXIS PHARM

    U.S.A
    ICHH-25
    Not Confirmed
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    U.S.A
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    ICHH-25
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEPHAPIRIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20GM BASE/VIAL

    Packaging :

    Approval Date : 1986-11-17

    Application Number : 62723

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Boehringer Ingelheim GmbH

    Germany
    ICHH-25
    Not Confirmed
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    Boehringer Ingelheim GmbH

    Germany
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    ICHH-25
    Not Confirmed
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    Regulatory Info : Prescription

    Registration Country : Canada

    CEPHAPIRIN (CEPHAPIRIN SODIUM)

    Brand Name : CEFA-LAK

    Dosage Form : SUSPENSION

    Dosage Strength : 200MG/10ML

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    Approval Date :

    Application Number : 2173263

    Regulatory Info : Prescription

    Registration Country : Canada

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    07

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50446

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50446

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
    arrow
    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50446

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
    arrow
    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50446

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50446

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
    arrow
    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61769

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61769

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/VIAL

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 61769

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1986-12-23

    Application Number : 62724

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1986-12-23

    Application Number : 62724

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1988-09-20

    Application Number : 62961

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1988-09-20

    Application Number : 62961

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1988-09-20

    Application Number : 62961

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    Bristol Myers Squibb

    U.S.A
    ICHH-25
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEFADYL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4GM BASE/VIAL

    Packaging :

    Approval Date : 1988-09-20

    Application Number : 62961

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    Hikma Pharmaceuticals

    United Kingdom
    ICHH-25
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    ICHH-25
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    Regulatory Info : DISCN

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    CEPHAPIRIN SODIUM

    Brand Name : CEPHAPIRIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 500MG BASE/VIAL

    Packaging :

    Approval Date : 1987-07-02

    Application Number : 62720

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Hikma Pharmaceuticals

    United Kingdom
    ICHH-25
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    ICHH-25
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEPHAPIRIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1GM BASE/VIAL

    Packaging :

    Approval Date : 1987-07-02

    Application Number : 62720

    Regulatory Info : DISCN

    Registration Country : USA

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    23

    Hikma Pharmaceuticals

    United Kingdom
    ICHH-25
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    ICHH-25
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    Regulatory Info : DISCN

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    CEPHAPIRIN SODIUM

    Brand Name : CEPHAPIRIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2GM BASE/VIAL

    Packaging :

    Approval Date : 1987-07-02

    Application Number : 62720

    Regulatory Info : DISCN

    Registration Country : USA

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    24

    Hikma Pharmaceuticals

    United Kingdom
    ICHH-25
    Not Confirmed
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    Hikma Pharmaceuticals

    United Kingdom
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    ICHH-25
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    CEPHAPIRIN SODIUM

    Brand Name : CEPHAPIRIN SODIUM

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20GM BASE/VIAL

    Packaging :

    Approval Date : 1987-07-02

    Application Number : 62720

    Regulatory Info : DISCN

    Registration Country : USA

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    25

    Qilu Animal Health Products

    China
    ICHH-25
    Not Confirmed
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    Qilu Animal Health Products

    China
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    ICHH-25
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info :

    Registration Country : China

    Cephapirin Sodium

    Brand Name :

    Dosage Form : Intramammary Infusion

    Dosage Strength : 200MG

    Packaging : 10 ml

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : China

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