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01 7Actavis Inc

02 2Ajanta Pharma Limited

03 2Aurolife Pharma LLC

04 2Avanthi Pharma

05 4ENDO OPERATIONS

06 3Endo International

07 12Endo Pharm

08 2Epic Pharma. LLC.

09 9Hikma Pharmaceuticals

10 7Impax Laboratories

11 9Mallinckrodt Pharmaceuticals

12 7Par Pharmaceutical

13 7Sun Pharmaceutical Industries Limited

14 2Teva Pharmaceutical Industries

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PharmaCompass

01

STLE Annual Meeting
Not Confirmed
arrow
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STLE Annual Meeting
Not Confirmed

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

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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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09

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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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10

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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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11

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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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12

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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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13

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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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14

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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

blank

15

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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

blank

16

STLE Annual Meeting
Not Confirmed
arrow
arrow
STLE Annual Meeting
Not Confirmed

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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17

ENDO OPERATIONS

Country
STLE Annual Meeting
Not Confirmed
arrow

ENDO OPERATIONS

Country
arrow
STLE Annual Meeting
Not Confirmed

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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18

ENDO OPERATIONS

Country
STLE Annual Meeting
Not Confirmed
arrow

ENDO OPERATIONS

Country
arrow
STLE Annual Meeting
Not Confirmed

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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19

ENDO OPERATIONS

Country
STLE Annual Meeting
Not Confirmed
arrow

ENDO OPERATIONS

Country
arrow
STLE Annual Meeting
Not Confirmed

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

20

ENDO OPERATIONS

Country
STLE Annual Meeting
Not Confirmed
arrow

ENDO OPERATIONS

Country
arrow
STLE Annual Meeting
Not Confirmed

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