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    Approved Drug Products containing Prestwick2_001102 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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    Prestwick2_001102

    ACTIVE PHARMA INGREDIENTS

    PRICE INFORMATION

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

    MARKET PLACE

    PATENTS & EXCLUSIVITIES

    REF. STANDARDS & IMPURITIES

    ANALYTICAL

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    $ API Ref.Price (USD/KG) : 249Xls

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    01 2CEPH INTL

    02 2CHARTWELL RX

    03 6DAVA PHARMS INC

    04 4FACTA FARMA

    05 2HIKMA

    06 6IVAX SUB TEVA PHARMS

    07 6LILLY

    08 6RANBAXY

    09 4RANBAXY LABS LTD

    10 6TEVA

    11 4WATSON LABS INC

    12 1WORLD GEN

    13 6YUNG SHIN PHARM

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    FACTA FARMA

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    RLD : No

    TE Code :

    CEFACLOR

    Brand Name : CEFACLOR

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 125MG BASE/5ML

    Approval Date : 1982-01-01

    Application Number : 62206

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    RLD : No

    TE Code :

    CEFACLOR

    Brand Name : CEFACLOR

    Dosage Form : FOR SUSPENSION;ORAL

    Dosage Strength : EQ 250MG BASE/5ML

    Approval Date : 1982-01-01

    Application Number : 62206

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    LILLY

    U.S.A
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    RLD : Yes

    TE Code :

    CEFACLOR

    Brand Name : CECLOR

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50521

    RX/OTC/DISCN : DISCN

    RLD : Yes

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    RLD : Yes

    TE Code :

    CEFACLOR

    Brand Name : CECLOR

    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 : 50521

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    05

    LILLY

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    RLD : Yes

    TE Code :

    CEFACLOR

    Brand Name : CECLOR

    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 : 50522

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    06

    LILLY

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    RLD : Yes

    TE Code :

    CEFACLOR

    Brand Name : CECLOR

    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 : 50522

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    07

    LILLY

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    RLD : No

    TE Code :

    CEFACLOR

    Brand Name : CECLOR CD

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 375MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1996-06-28

    Application Number : 50673

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    RLD : No

    TE Code :

    CEFACLOR

    Brand Name : CECLOR CD

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

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

    Approval Date : 1996-06-28

    Application Number : 50673

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    CEPH INTL

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    RLD : No

    TE Code :

    CEFACLOR

    Brand Name : CEFACLOR

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 250MG BASE

    Approval Date : 1982-01-01

    Application Number : 62205

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    CEPH INTL

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    RLD : No

    TE Code :

    CEFACLOR

    Brand Name : CEFACLOR

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 500MG BASE

    Approval Date : 1982-01-01

    Application Number : 62205

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

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