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:
Approved
Current status date:
2025-10-09
Product name:
OPUVIZ
Description:
SINGLE-USE PRE-FILLED SYRINGE
DIN:
02561883
Product Monograph/Veterinary Labelling:
Date:
2025-10-06
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
SAMSUNG BIOEPIS CO., LTD
76, Songdogyoyuk-Ro, Yeonsu-Gu
Incheon
Incheon
Korea, Republic Of
21987
Class:
Human
Dosage form(s):
Solution
Route(s) of administration:
Intravitreal
Number of active ingredient(s):
1
Schedule(s):
SCHEDULE D , PRESCRIPTION
Biosimilar Biologic Drug:
Yes
Anatomical Therapeutic Chemical (ATC): See footnote 4
S01LA05 AFLIBERCEPT
Active ingredient group (AIG) number:See footnote5
0154950001
| Active ingredient(s) See footnote8 | Strength |
|---|---|
| AFLIBERCEPT | 2 MG / 0.05 ML |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.