Product information
From Health Canada
No match found
No other product was found with the same active ingredient group.
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:
Cancelled Pre Market
Current status date:
2017-03-16
Original market date: See footnote 1
Product name:
OPANA ER
DIN:
02383438
Product Monograph/Veterinary Labelling:
Date:
2016-06-21
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
PALADIN PHARMA INC.
100 Blvd Alexis-Nihon, Suite 600
Saint-Laurent
Quebec
Canada
H4M 2P2
Class:
Human
Dosage form(s):
Tablet (Extended-Release)
Route(s) of administration:
Oral
Number of active ingredient(s):
1
Schedule(s):
Narcotic (CDSA I)
American Hospital Formulary Service (AHFS): See footnote 3
28:08.08
Anatomical Therapeutic Chemical (ATC): See footnote 4
N02AA NATURAL OPIUM ALKALOIDS
Active ingredient group (AIG) number:See footnote5
0107554004
| Active ingredient(s) | Strength |
|---|---|
| OXYMORPHONE HYDROCHLORIDE | 10 MG |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.