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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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    xyz-pharma-m-2025-03-24

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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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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    xyz-pharma-m-2025-03-17

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    Folotyn

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    01 2DR REDDYS

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    03 2TEVA PHARMS USA INC

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    DR REDDYS

    India
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    CPhI Japan
    Booth #5N-12
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    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    RLD : No

    TE Code : AP

    PRALATREXATE

    Brand Name : PRALATREXATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 20MG/ML (20MG/ML)

    Approval Date : 2025-03-10

    Application Number : 206183

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    DR REDDYS

    India
    arrow
    CPhI Japan
    Booth #5N-12
    • fda
    • EDQM
    • WHO-GMP

    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    RLD : No

    TE Code : AP

    PRALATREXATE

    Brand Name : PRALATREXATE

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 40MG/2ML (20MG/ML)

    Approval Date : 2025-03-10

    Application Number : 206183

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    ACROTECH BIOPHARMA

    U.S.A
    Plastics Recycling EU
    Not Confirmed
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    ACROTECH BIOPHARMA

    U.S.A
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    Plastics Recycling EU
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code : AP

    PRALATREXATE

    Brand Name : FOLOTYN

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 20MG/ML (20MG/ML)

    Approval Date : 2009-09-24

    Application Number : 22468

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    04

    ACROTECH BIOPHARMA

    U.S.A
    Plastics Recycling EU
    Not Confirmed
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    ACROTECH BIOPHARMA

    U.S.A
    arrow
    Plastics Recycling EU
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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 : AP

    PRALATREXATE

    Brand Name : FOLOTYN

    Dosage Form : SOLUTION;INTRAVENOUS

    Dosage Strength : 40MG/2ML (20MG/ML)

    Approval Date : 2009-09-24

    Application Number : 22468

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    05

    TEVA PHARMS USA INC

    Israel
    Plastics Recycling EU
    Not Confirmed
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    TEVA PHARMS USA INC

    Israel
    arrow
    Plastics Recycling EU
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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 :

    TE Code :

    PRALATREXATE

    Brand Name : PRALATREXATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 20MG/1ML

    Approval Date :

    Application Number : 206167

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    06

    TEVA PHARMS USA INC

    Israel
    Plastics Recycling EU
    Not Confirmed
    arrow

    TEVA PHARMS USA INC

    Israel
    arrow
    Plastics Recycling EU
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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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    Flag Israel
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    RLD :

    TE Code :

    PRALATREXATE

    Brand Name : PRALATREXATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/2ML

    Approval Date :

    Application Number : 206167

    RX/OTC/DISCN :

    RLD :

    TE Code :

    blank

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