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    01 5Actavis Inc

    02 8Ajanta Pharma Limited

    03 4Apotex Inc

    04 7Aristo Pharma GmbH

    05 2Ascent Pharmaceuticals

    06 3Aurolife Pharma LLC

    07 1Barr Laboratories

    08 4Chartwell Pharmaceuticals llc

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    11 7Fresenius Kabi USA

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    21 2Lannett Company, Inc.

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    24 7Medsurge Healthcare

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    30 11Pharmascience Inc.

    31 12Purdue Pharma

    32 4Purdue Pharmaceuticals L.P

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    01

    Actavis Inc

    Ireland
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    Regulatory Info : DISCN

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : HYDROMORPHONE HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

    Packaging :

    Approval Date : 1995-08-23

    Application Number : 74317

    Regulatory Info : DISCN

    Registration Country : USA

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    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : DISCN

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID-HP

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 10MG/ML

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    Approval Date : 1984-01-11

    Application Number : 19034

    Regulatory Info : DISCN

    Registration Country : USA

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    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : DISCN

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID-HP

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 250MG/VIAL

    Packaging :

    Approval Date : 1994-08-04

    Application Number : 19034

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 1MG/ML

    Packaging :

    Approval Date : 2009-04-30

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    05

    Fresenius Kabi USA

    U.S.A
    AIChE Annual Meeting
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    Regulatory Info : RX

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 2MG/ML

    Packaging :

    Approval Date : 2009-04-30

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    06

    Fresenius Kabi USA

    U.S.A
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    Regulatory Info : RX

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 4MG/ML

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    Approval Date : 2009-04-30

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    07

    Fresenius Kabi USA

    U.S.A
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.2MG/ML

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    Approval Date : 2020-01-16

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    Fresenius Kabi USA

    U.S.A
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.5MG/0.5ML

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    Approval Date : 2017-02-10

    Application Number : 19034

    Regulatory Info : RX

    Registration Country : USA

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    09

    Mallinckrodt Pharmaceuticals

    Ireland
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : EXALGO

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2010-03-01

    Application Number : 21217

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Mallinckrodt Pharmaceuticals

    Ireland
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : EXALGO

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2010-03-01

    Application Number : 21217

    Regulatory Info : DISCN

    Registration Country : USA

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    Mallinckrodt Pharmaceuticals

    Ireland
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : EXALGO

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 16MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2010-03-01

    Application Number : 21217

    Regulatory Info : DISCN

    Registration Country : USA

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    Mallinckrodt Pharmaceuticals

    Ireland
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : EXALGO

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 32MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 2012-08-24

    Application Number : 21217

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Purdue Pharmaceuticals L.P

    U.S.A
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : PALLADONE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 12MG

    Packaging :

    Approval Date : 2004-09-24

    Application Number : 21044

    Regulatory Info : DISCN

    Registration Country : USA

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    Purdue Pharmaceuticals L.P

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    Brand Name : PALLADONE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 16MG

    Packaging :

    Approval Date : 2004-09-24

    Application Number : 21044

    Regulatory Info : DISCN

    Registration Country : USA

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    Purdue Pharmaceuticals L.P

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : PALLADONE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 24MG

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    Approval Date : 2004-09-24

    Application Number : 21044

    Regulatory Info : DISCN

    Registration Country : USA

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    Purdue Pharmaceuticals L.P

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    Brand Name : PALLADONE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 32MG

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    Approval Date : 2004-09-24

    Application Number : 21044

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    RHODES PHARMACEUTICALS LP

    U.S.A
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 5MG/5ML

    Packaging :

    Approval Date : 1992-12-07

    Application Number : 19891

    Regulatory Info : RX

    Registration Country : USA

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    RHODES PHARMACEUTICALS LP

    U.S.A
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    Regulatory Info : RX

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 8MG

    Packaging :

    Approval Date : 1992-12-07

    Application Number : 19892

    Regulatory Info : RX

    Registration Country : USA

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    RHODES PHARMACEUTICALS LP

    U.S.A
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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 4MG

    Packaging :

    Approval Date : 2007-11-09

    Application Number : 19892

    Regulatory Info : RX

    Registration Country : USA

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    RHODES PHARMACEUTICALS LP

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    HYDROMORPHONE HYDROCHLORIDE

    Brand Name : DILAUDID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Packaging :

    Approval Date : 2007-11-09

    Application Number : 19892

    Regulatory Info : RX

    Registration Country : USA

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