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The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.

Current status:

Marketed

Current status date:

2011-09-13

Original market date: See footnote 1

2011-09-13

Product name:

OXYNEO

Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section .

DIN:

02372525

Product Monograph/Veterinary Labelling:

Date: 2020-08-31 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company: 

PURDUE PHARMA
575 Granite Court
Pickering
Ontario
Canada  L1W 3W8

Class: 

Human

Dosage form(s):

Tablet (Extended-Release)

Route(s) of administration:

Oral

Number of active ingredient(s):

1

Schedule(s):

Narcotic (CDSA I)  

Biosimilar Biologic Drug:

No

American Hospital Formulary Service (AHFS): See footnote 3

28:08.08   OPIATE AGONISTS

Anatomical Therapeutic Chemical (ATC): See footnote 4

N02AA05  OXYCODONE

Active ingredient group (AIG) number:See footnote 5

0107552002

List of active ingredient(s)
Active ingredient(s) Strength
OXYCODONE HYDROCHLORIDE 10 MG

Risk Management Plans See footnote 7

A Risk Management Plan (RMP) for this product was submitted.

A Canadian Specific Opioid targeted Risk Management Plan (CSO-tRMP) for this product was submitted.

Additional Risk Minimization Measures
Healthcare Professional Education
Pharmacovigilance/Monitoring Activity
Drug Utilisation Study (DUS) study

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