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    Approved Drug Products containing CEFADROXIL/CEFADROXIL HEMIHYDRATE listed in the FDA Orange Book. Original Data : FDA Website

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

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    xyz-pharma-m-2024-09-09

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    Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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

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    xyz-pharma-m-2024-09-09

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    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    ACTIVE PHARMA INGREDIENTS

    PRICE INFORMATION

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

    ANALYTICAL

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    $ API Ref.Price (USD/KG) : 67Xls

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    01 5ANI PHARMS

    02 4APOTHECON

    03 2AUROBINDO

    04 1AUROBINDO PHARMA

    05 5BRISTOL

    06 4CHARTWELL RX

    07 1CSPC OUYI

    08 2HIKMA

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    10 1IVAX SUB TEVA PHARMS

    11 3LUPIN

    12 1PUREPAC PHARM

    13 1RANBAXY

    14 1RANBAXY LABS LTD

    15 1SANDOZ

    16 3SUN PHARM INDS LTD

    17 1TEVA

    18 2TEVA PHARMS

    19 6WARNER CHILCOTT

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    01

    APOTHECON

    U.S.A
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    APOTHECON

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    RLD : No

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 125MG BASE/5ML

    Approval Date : 1982-01-01

    Application Number : 62334

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    APOTHECON

    U.S.A
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    APOTHECON

    U.S.A
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    RLD : No

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

    Approval Date : 1982-01-01

    Application Number : 62334

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    03

    APOTHECON

    U.S.A
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    APOTHECON

    U.S.A
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    RLD : No

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : CEFADROXIL

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 500MG BASE/5ML

    Approval Date : 1982-01-01

    Application Number : 62334

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    SANDOZ

    Switzerland
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    05

    WARNER CHILCOTT

    U.S.A
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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50512

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    06

    WARNER CHILCOTT

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    RLD : No

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE

    Approval Date : 1982-01-01

    Application Number : 50512

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    WARNER CHILCOTT

    U.S.A
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    WARNER CHILCOTT

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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 500MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50527

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    08

    WARNER CHILCOTT

    U.S.A
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    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 125MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50527

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    09

    WARNER CHILCOTT

    U.S.A
    Formnext Forum
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    Not Confirmed
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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50527

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

    Portfolio PDF

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    10

    WARNER CHILCOTT

    U.S.A
    Formnext Forum
    Not Confirmed
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    WARNER CHILCOTT

    U.S.A
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    Formnext Forum
    Not Confirmed
    • fda
    • EDQM
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code :

    CEFADROXIL/CEFADROXIL HEMIHYDRATE

    Brand Name : DURICEF

    Dosage Form : TABLET;ORAL

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

    Approval Date : 1982-01-01

    Application Number : 50528

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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