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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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    Oxymorphone HCl

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    03 2Aurolife Pharma LLC

    04 2Avanthi Pharma

    05 7ENDO OPERATIONS

    06 12Endo Pharm

    07 2Epic Pharma. LLC.

    08 9Hikma Pharmaceuticals

    09 7Impax Laboratories

    10 9Mallinckrodt Pharmaceuticals

    11 7Par Pharmaceutical

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 7.5MG

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    Approval Date : 2010-12-13

    Application Number : 79046

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    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 15MG

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    Approval Date : 2010-12-13

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    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 5MG

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    Approval Date : 2013-07-11

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    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

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    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 20MG

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    Approval Date : 2013-07-11

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    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG

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    Approval Date : 2013-07-11

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    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 40MG

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    Approval Date : 2013-07-11

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1.5MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11707

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    Registration Country : USA

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    Brand Name : OPANA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11707

    Regulatory Info : DISCN

    Registration Country : USA

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    Endo Pharm

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : NUMORPHAN

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11738

    Regulatory Info : DISCN

    Registration Country : USA

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA

    Dosage Form : TABLET;ORAL

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

    Packaging :

    Approval Date : 2006-06-22

    Application Number : 21611

    Regulatory Info : DISCN

    Registration Country : USA

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    Endo Pharm

    Ireland
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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2006-06-22

    Application Number : 21611

    Regulatory Info : DISCN

    Registration Country : USA

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    Hikma Pharmaceuticals

    United Kingdom
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    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2010-09-27

    Application Number : 90964

    Regulatory Info : RX

    Registration Country : USA

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    Hikma Pharmaceuticals

    United Kingdom
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    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2010-09-27

    Application Number : 90964

    Regulatory Info : RX

    Registration Country : USA

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    Impax Laboratories

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    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2010-06-14

    Application Number : 79087

    Regulatory Info : RX

    Registration Country : USA

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    Impax Laboratories

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 7.5MG

    Packaging :

    Approval Date : 2010-12-21

    Application Number : 79087

    Regulatory Info : RX

    Registration Country : USA

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    Impax Laboratories

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    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2010-06-14

    Application Number : 79087

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    Registration Country : USA

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    Impax Laboratories

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2010-12-21

    Application Number : 79087

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    Registration Country : USA

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    Impax Laboratories

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2010-06-14

    Application Number : 79087

    Regulatory Info : RX

    Registration Country : USA

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    Impax Laboratories

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 2010-07-22

    Application Number : 79087

    Regulatory Info : RX

    Registration Country : USA

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    Impax Laboratories

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    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 2010-06-14

    Application Number : 79087

    Regulatory Info : RX

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    Teva Pharmaceutical Industries

    Israel
    Pharma, Lab & Chemical Expo
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    Israel
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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2011-02-15

    Application Number : 91443

    Regulatory Info : RX

    Registration Country : USA

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    Teva Pharmaceutical Industries

    Israel
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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2011-02-15

    Application Number : 91443

    Regulatory Info : RX

    Registration Country : USA

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    24

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    ENDO OPERATIONS

    Country
    arrow
    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA ER

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

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

    Packaging :

    Approval Date : 2006-06-22

    Application Number : 21610

    Regulatory Info : DISCN

    Registration Country : USA

    blank

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    Virtual Booth

    Digital Content

    Website

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    25

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    Pharma, Lab & Chemical Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA ER

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2006-06-22

    Application Number : 21610

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

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    Virtual Booth

    Digital Content

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    26

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    ENDO OPERATIONS

    Country
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    Pharma, Lab & Chemical Expo
    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

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA ER

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2006-06-22

    Application Number : 21610

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    27

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    ENDO OPERATIONS

    Country
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    Pharma, Lab & Chemical Expo
    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

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA ER

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2006-06-22

    Application Number : 21610

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    28

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    ENDO OPERATIONS

    Country
    arrow
    Pharma, Lab & Chemical Expo
    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

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA ER

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2008-02-29

    Application Number : 21610

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    29

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    ENDO OPERATIONS

    Country
    arrow
    Pharma, Lab & Chemical Expo
    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

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA ER

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2008-02-29

    Application Number : 21610

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

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    Virtual Booth

    Digital Content

    Website

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    30

    ENDO OPERATIONS

    Country
    Pharma, Lab & Chemical Expo
    Not Confirmed
    arrow

    ENDO OPERATIONS

    Country
    arrow
    Pharma, Lab & Chemical Expo
    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

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA ER

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2008-02-29

    Application Number : 21610

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

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    Virtual Booth

    Digital Content

    Website

    Corporate PDF