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    List of All Manufacturers & Suppliers of Oxymorphone HCl Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    Oxymorphone HCl

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    DRUG PRODUCT COMPOSITIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

    PATENTS & EXCLUSIVITIES

    REF. STANDARDS & IMPURITIES

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    01 7Actavis Inc

    02 2Ajanta Pharma Limited

    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

    12 7Sun Pharmaceutical Industries Limited

    13 2Teva Pharmaceutical Industries

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    01

    Actavis Inc

    Ireland
    Discovery on Target
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    Actavis Inc

    Ireland
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    Regulatory Info : DISCN

    Registration Country : USA

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 7.5MG

    Packaging :

    Approval Date : 2010-12-13

    Application Number : 79046

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Actavis Inc

    Ireland
    Discovery on Target
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    Actavis Inc

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    Discovery on Target
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    Regulatory Info : DISCN

    Registration Country : USA

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2010-12-13

    Application Number : 79046

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Actavis Inc

    Ireland
    Discovery on Target
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    Actavis Inc

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    Regulatory Info : DISCN

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2013-07-11

    Application Number : 79046

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Actavis Inc

    Ireland
    Discovery on Target
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    Actavis Inc

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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2013-07-11

    Application Number : 79046

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Actavis Inc

    Ireland
    Discovery on Target
    Not Confirmed
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    Actavis Inc

    Ireland
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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2013-07-11

    Application Number : 79046

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Actavis Inc

    Ireland
    Discovery on Target
    Not Confirmed
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    Actavis Inc

    Ireland
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    Discovery on Target
    Not Confirmed
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 2013-07-11

    Application Number : 79046

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Actavis Inc

    Ireland
    Discovery on Target
    Not Confirmed
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    Actavis Inc

    Ireland
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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 2013-07-11

    Application Number : 79046

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Endo Pharm

    Ireland
    Discovery on Target
    Not Confirmed
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    Endo Pharm

    Ireland
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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

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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

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Endo Pharm

    Ireland
    Discovery on Target
    Not Confirmed
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    Endo Pharm

    Ireland
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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

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    OXYMORPHONE HYDROCHLORIDE

    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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    10

    Endo Pharm

    Ireland
    Discovery on Target
    Not Confirmed
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    Endo Pharm

    Ireland
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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    11

    Endo Pharm

    Ireland
    Discovery on Target
    Not Confirmed
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    Endo Pharm

    Ireland
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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    12

    Endo Pharm

    Ireland
    Discovery on Target
    Not Confirmed
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    Endo Pharm

    Ireland
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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    13

    Impax Laboratories

    U.S.A
    Discovery on Target
    Not Confirmed
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    Impax Laboratories

    U.S.A
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    Discovery on Target
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    Regulatory Info : RX

    Registration Country : USA

    OXYMORPHONE HYDROCHLORIDE

    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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    14

    ENDO OPERATIONS

    Country
    Discovery on Target
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    ENDO OPERATIONS

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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

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    15

    ENDO OPERATIONS

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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

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    16

    ENDO OPERATIONS

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    Discovery on Target
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    ENDO OPERATIONS

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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

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    17

    ENDO OPERATIONS

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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

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    18

    ENDO OPERATIONS

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    ENDO OPERATIONS

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    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

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    19

    ENDO OPERATIONS

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    ENDO OPERATIONS

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    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

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    20

    ENDO OPERATIONS

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    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

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