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:
Marketed
Current status date:
2018-09-21
Original market date: See footnote 1
2018-09-21
Product name:
MORPHINE SULFATE INJECTION BP
DIN:
02474980
Product Monograph/Veterinary Labelling:
Date:
2018-04-20
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
STERIMAX INC
2770 Portland Drive
Oakville
Ontario
Canada
L6H 6R4
Class:
Human
Dosage form(s):
Solution
Route(s) of administration:
Intravenous , Subcutaneous , Intramuscular
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
N02AA01 MORPHINE
Active ingredient group (AIG) number:See footnote5
0104545001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| MORPHINE SULFATE | 10 MG / ML |
Risk Management Plans See footnote 7
A Canadian Specific Opioid targeted Risk Management Plan (CSO-tRMP) for this product was submitted.
| Additional Risk Minimization Measures |
|---|
| Healthcare Professional Education |