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 Post Market
Current status date:
2023-06-30
Original market date: See footnote 1
2018-11-22
Lot number: See footnote 2
RHCC-B
Expiry date: See footnote 2
2023-06-30
Product name:
PROBUPHINE
DIN:
02474921
Product Monograph/Veterinary Labelling:
Date:
2020-05-20
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
KNIGHT THERAPEUTICS INC.
1055
3400 De Maisonneuve Blvd W
Montreal
Quebec
Canada
H3Z 3B8
Class:
Human
Dosage form(s):
Implant
Route(s) of administration:
Subcutaneous
Number of active ingredient(s):
1
Schedule(s):
Narcotic (CDSA I)
American Hospital Formulary Service (AHFS): See footnote 3
28:08.12
Anatomical Therapeutic Chemical (ATC): See footnote 4
N07BC01 BUPRENORPHINE
Active ingredient group (AIG) number:See footnote5
0126788005
Active ingredient(s) | Strength |
---|---|
BUPRENORPHINE HYDROCHLORIDE | 80 MG |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.
Additional Risk Minimization Measures |
---|
Controlled Distribution Program |