Product information
From Health Canada
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 Post Market
Current status date:
2014-06-20
Original market date: See footnote 1
2004-04-06
Product name:
HYDROMORPHONE
DIN:
02192101
Product Monograph/Veterinary Labelling:
Date:
2012-03-29
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
SORRES PHARMA INC
SUITE 100
6111 Royalmount Ave
Montreal
Quebec
Canada
H4P 2T4
Class:
Human
Dosage form(s):
Tablet
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
N02AA03 HYDROMORPHONE
Active ingredient group (AIG) number:See footnote5
0108698004
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| HYDROMORPHONE HYDROCHLORIDE | 1 MG |