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:

2022-06-27

Original market date: See footnote 1

2022-06-27

Product name:

AYBINTIO

Description:

SINGLE USE VIAL

Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section.

DIN:

02522829

Product Monograph/Veterinary Labelling:

Date: 2023-01-30 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:

Intravenous

Number of active ingredient(s):

1

Schedule(s):

Schedule D ,  Prescription Recommended

Biosimilar Biologic Drug:

Yes

American Hospital Formulary Service (AHFS): See footnote 3

10:00.00 

Anatomical Therapeutic Chemical (ATC): See footnote 4

L01FG01 BEVACIZUMAB

Active ingredient group (AIG) number:See footnote5

0151381001

List of active ingredient(s)
Active ingredient(s) Strength
BEVACIZUMAB 100 MG / 4 ML

Risk Management Plans See footnote 7

A Risk Management Plan (RMP) for this product was submitted.

Version 4.0.2
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