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

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    xyz-pharma-m-2024-10-07

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    02 7AstraZeneca

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    01

    Amneal Pharmaceuticals

    U.S.A
    Antibody Engineering
    Not Confirmed
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    Amneal Pharmaceuticals

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    • EDQM
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    Regulatory Info :

    Registration Country : USA

    EXENATIDE SYNTHETIC

    Brand Name : EXENATIDE SYNTHETIC

    Dosage Form : INJECTABLE;SUBCUTANEOUS

    Dosage Strength : 300MCG/1.2ML (250MCG/ML)

    Packaging :

    Approval Date :

    Application Number : 206697

    Regulatory Info :

    Registration Country : USA

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    02

    Amneal Pharmaceuticals

    U.S.A
    Antibody Engineering
    Not Confirmed
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    Amneal Pharmaceuticals

    U.S.A
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    Antibody Engineering
    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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    Regulatory Info :

    Registration Country : USA

    EXENATIDE SYNTHETIC

    Brand Name : EXENATIDE SYNTHETIC

    Dosage Form : INJECTABLE;SUBCUTANEOUS

    Dosage Strength : 600MCG/2.4ML (250MCG/ML)

    Packaging :

    Approval Date :

    Application Number : 206697

    Regulatory Info :

    Registration Country : USA

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    03

    AstraZeneca

    United Kingdom
    Antibody Engineering
    Not Confirmed
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    AstraZeneca

    United Kingdom
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    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    EXENATIDE SYNTHETIC

    Brand Name : BYETTA

    Dosage Form : INJECTABLE;SUBCUTANEOUS

    Dosage Strength : 300MCG/1.2ML (250MCG/ML)

    Packaging :

    Approval Date : 2005-04-28

    Application Number : 21773

    Regulatory Info : RX

    Registration Country : USA

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    04

    AstraZeneca

    United Kingdom
    Antibody Engineering
    Not Confirmed
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    AstraZeneca

    United Kingdom
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    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    EXENATIDE SYNTHETIC

    Brand Name : BYETTA

    Dosage Form : INJECTABLE;SUBCUTANEOUS

    Dosage Strength : 600MCG/2.4ML (250MCG/ML)

    Packaging :

    Approval Date : 2005-04-28

    Application Number : 21773

    Regulatory Info : RX

    Registration Country : USA

    blank

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    Website

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    05

    AstraZeneca

    United Kingdom
    Antibody Engineering
    Not Confirmed
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    AstraZeneca

    United Kingdom
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    Antibody Engineering
    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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    Regulatory Info :

    Registration Country : USA

    EXENATIDE SYNTHETIC

    Brand Name : BYETTA

    Dosage Form : INJECTABLE; SUBCUTANEOUS

    Dosage Strength : 300UGM/1.2ML (250UGM/ML)

    Packaging :

    Approval Date :

    Application Number : 21919

    Regulatory Info :

    Registration Country : USA

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    06

    AstraZeneca

    United Kingdom
    Antibody Engineering
    Not Confirmed
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    AstraZeneca

    United Kingdom
    arrow
    Antibody Engineering
    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 United Kingdom
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info :

    Registration Country : USA

    EXENATIDE SYNTHETIC

    Brand Name : BYETTA

    Dosage Form : INJECTABLE; SUBCUTANEOUS

    Dosage Strength : 600UGM/2.4ML (250UGM/ML)

    Packaging :

    Approval Date :

    Application Number : 21919

    Regulatory Info :

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

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    07

    AstraZeneca

    United Kingdom
    Antibody Engineering
    Not Confirmed
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    AstraZeneca

    United Kingdom
    arrow
    Antibody Engineering
    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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    Regulatory Info : DISCN

    Registration Country : USA

    EXENATIDE SYNTHETIC

    Brand Name : BYDUREON

    Dosage Form : FOR SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS

    Dosage Strength : 2MG/VIAL

    Packaging :

    Approval Date : 2012-01-27

    Application Number : 22200

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    AstraZeneca

    United Kingdom
    Antibody Engineering
    Not Confirmed
    arrow

    AstraZeneca

    United Kingdom
    arrow
    Antibody Engineering
    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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    Regulatory Info : DISCN

    Registration Country : USA

    EXENATIDE SYNTHETIC

    Brand Name : BYDUREON PEN

    Dosage Form : FOR SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS

    Dosage Strength : 2MG

    Packaging :

    Approval Date : 2014-02-28

    Application Number : 22200

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

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    09

    AstraZeneca

    United Kingdom
    Antibody Engineering
    Not Confirmed
    arrow

    AstraZeneca

    United Kingdom
    arrow
    Antibody Engineering
    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.
    Post an Enquiry Post an Enquiry
    Flag United Kingdom
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    EXENATIDE SYNTHETIC

    Brand Name : BYDUREON BCISE

    Dosage Form : SUSPENSION, EXTENDED RELEASE;SUBCUTANEOUS

    Dosage Strength : 2MG/0.85ML (2MG/0.85ML)

    Packaging :

    Approval Date : 2017-10-20

    Application Number : 209210

    Regulatory Info : RX

    Registration Country : USA

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