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    Oxymorphone HCl

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    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 7.5MG

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    Approval Date : 2010-12-13

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    OXYMORPHONE HYDROCHLORIDE

    Brand Name : OPANA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1.5MG/ML

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    Approval Date : 1982-01-01

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    Brand Name : OPANA

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1MG/ML

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    Approval Date : 1982-01-01

    Application Number : 11707

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    Registration Country : USA

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    Brand Name : NUMORPHAN

    Dosage Form : SUPPOSITORY;RECTAL

    Dosage Strength : 5MG

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    Approval Date : 1982-01-01

    Application Number : 11738

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    Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2006-06-22

    Application Number : 21611

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    Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2006-06-22

    Application Number : 21611

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    Brand Name : OXYMORPHONE HYDROCHLORIDE

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 5MG

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    Approval Date : 2010-06-14

    Application Number : 79087

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    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2006-06-22

    Application Number : 21610

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

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    Approval Date : 2006-06-22

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    Brand Name : OPANA ER

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

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

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    Approval Date : 2006-06-22

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

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    Approval Date : 2008-02-29

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

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    Approval Date : 2008-02-29

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    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**

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    Approval Date : 2008-02-29

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