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Oxymorphone Hydrochloride
FDF Dossiers

DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.

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pharmacompass-1-m-2026-01-12

LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.https://marketing.lgmpharma.com/LGM-CDMO

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Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.

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pharmacompass-2-2026-02-09

Oxymorphone Hydrochloride

ACCESS ALL DATA, CHEMISTRY

ACCESS ALL DATA
CHEMISTRY
Discover Molecule Insights

ACTIVE PHARMA INGREDIENTS

8 API Suppliers, 6 USDMF, 3 NDC API, 5 Listed Suppliers

8 API Suppliers
6 USDMF
3 NDC API
5 Listed Suppliers

DEVELOPMENTS

3 Drugs in Development

3 Drugs in Development

FINISHED DOSAGE FORMULATIONS

75 FDF Dossiers, 75 FDA Orange Book

75 FDF Dossiers
75 FDA Orange Book

DRUG PRODUCT COMPOSITIONS

INJECTABLE;INJECTION - 1MG/ML, TABLET, EXTENDED RELEASE;ORAL - 10MG, TABLET, EXTENDED RELEASE;ORAL - 15MG, TABLET, EXTENDED RELEASE;ORAL - 20MG, TABLET, EXTENDED RELEASE;ORAL - 30MG, TABLET, EXTENDED RELEASE;ORAL - 40MG, TABLET, EXTENDED RELEASE;ORAL - 5MG, TABLET, EXTENDED RELEASE;ORAL - 7.5MG, TABLET, EXTENDED RELEASE;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET, EXTENDED RELEASE;ORAL - 7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, TABLET;ORAL - 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

INJECTABLE;INJECTION - 1MG/ML
TABLET, EXTENDED RELEASE;ORAL - 10MG
TABLET, EXTENDED RELEASE;ORAL - 15MG
TABLET, EXTENDED RELEASE;ORAL - 20MG
TABLET, EXTENDED RELEASE;ORAL - 30MG
TABLET, EXTENDED RELEASE;ORAL - 40MG
TABLET, EXTENDED RELEASE;ORAL - 5MG
TABLET, EXTENDED RELEASE;ORAL - 7.5MG
TABLET, EXTENDED RELEASE;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET, EXTENDED RELEASE;ORAL - 7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
TABLET;ORAL - 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

DIGITAL CONTENT

15 News #PharmaBuzz

15 News #PharmaBuzz

GLOBAL SALES INFORMATION

5 US Medicaid Prescriptions, 17 Regulatory FDF Prices

5 US Medicaid Prescriptions
17 Regulatory FDF Prices

PATENTS & EXCLUSIVITIES

42 US Patents

42 US Patents

REF. STANDARDS & IMPURITIES

2 Others

2 Others

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filter Applicant Reset all filters

75 All

01 7Actavis Inc

02 2Ajanta Pharma Limited

03 2Aurolife Pharma LLC

04 2Avanthi Pharma

05 7Endo International

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

filter Dosage Reset all filters

75 All

01 2INJECTABLE;INJECTION

02 1SUPPOSITORY;RECTAL

03 56TABLET, EXTENDED RELEASE;ORAL

04 16TABLET;ORAL

filter Regulatory Info Reset all filters

75 All

01 56DISCN

02 19RX

filter Brand Name Reset all filters

75 All

01 1NUMORPHAN

02 4OPANA

03 14OPANA ER

04 56OXYMORPHONE HYDROCHLORIDE

filter Country Reset all filters

75 All

01 75USA

List of Suppliers

Product Main Page

01

Actavis Inc

International Sweetener Colloquium

Not Confirmed

Actavis Inc

International Sweetener Colloquium

Not Confirmed

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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Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

02

Actavis Inc

International Sweetener Colloquium

Not Confirmed

Actavis Inc

International Sweetener Colloquium

Not Confirmed

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Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

03

Actavis Inc

International Sweetener Colloquium

Not Confirmed

Actavis Inc

International Sweetener Colloquium

Not Confirmed

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Digital Content

Regulatory Info : DISCN

Registration Country : USA

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

04

Actavis Inc

International Sweetener Colloquium

Not Confirmed

Actavis Inc

International Sweetener Colloquium

Not Confirmed

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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Digital Content

Regulatory Info : DISCN

Registration Country : USA

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

05

Actavis Inc

International Sweetener Colloquium

Not Confirmed

Actavis Inc

International Sweetener Colloquium

Not Confirmed

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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Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

06

Actavis Inc

International Sweetener Colloquium

Not Confirmed

Actavis Inc

International Sweetener Colloquium

Not Confirmed

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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Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

07

Actavis Inc

International Sweetener Colloquium

Not Confirmed

Actavis Inc

International Sweetener Colloquium

Not Confirmed

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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Digital Content

Regulatory Info : DISCN

Registration Country : USA

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

08

Endo International

International Sweetener Colloquium

Not Confirmed

Endo International

International Sweetener Colloquium

Not Confirmed

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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Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

09

Endo International

International Sweetener Colloquium

Not Confirmed

Endo International

International Sweetener Colloquium

Not Confirmed

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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Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

10

Endo International

International Sweetener Colloquium

Not Confirmed

Endo International

International Sweetener Colloquium

Not Confirmed

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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Post an Enquiry

Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

11

Endo International

International Sweetener Colloquium

Not Confirmed

Endo International

International Sweetener Colloquium

Not Confirmed

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.

Post an Enquiry

Post an Enquiry

Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

12

Endo International

International Sweetener Colloquium

Not Confirmed

Endo International

International Sweetener Colloquium

Not Confirmed

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.

Post an Enquiry

Post an Enquiry

Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

13

Endo International

International Sweetener Colloquium

Not Confirmed

Endo International

International Sweetener Colloquium

Not Confirmed

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.

Post an Enquiry

Post an Enquiry

Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

14

Endo International

International Sweetener Colloquium

Not Confirmed

Endo International

International Sweetener Colloquium

Not Confirmed

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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Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

15

Endo Pharm

International Sweetener Colloquium

Not Confirmed

Endo Pharm

International Sweetener Colloquium

Not Confirmed

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Regulatory Info : DISCN

Registration Country : USA

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

Portfolio PDF

Product Web Link

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16

Endo Pharm

International Sweetener Colloquium

Not Confirmed

Endo Pharm

International Sweetener Colloquium

Not Confirmed

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Digital Content

Regulatory Info : DISCN

Registration Country : USA

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

17

Endo Pharm

International Sweetener Colloquium

Not Confirmed

Endo Pharm

International Sweetener Colloquium

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

Portfolio PDF

Product Web Link

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Corporate PDF

18

Endo Pharm

International Sweetener Colloquium

Not Confirmed

Endo Pharm

International Sweetener Colloquium

Not Confirmed

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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Post an Enquiry

Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

19

Endo Pharm

International Sweetener Colloquium

Not Confirmed

Endo Pharm

International Sweetener Colloquium

Not Confirmed

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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Digital Content

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

Portfolio PDF

Product Web Link

Digital Content

Corporate PDF

20

Impax Laboratories

International Sweetener Colloquium

Not Confirmed

Impax Laboratories

International Sweetener Colloquium

Not Confirmed

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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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Product Web Link

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Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.