Product List
Here is an overview of our products.
Australia Consumer Medicine Information
Please Note: The storage temperature for Alburex® 5 AU has been updated to storage below 30°C. Product labelled with the updated storage temperature will be available approximately June 2025.
Product currently supplied and in circulation labelled with storage below 25°C is still appropriate to use.
Australia Consumer Medicine Information
Please Note: The storage temperature for Alburex® 20 AU has been updated to storage below 30°C. Product labelled with the updated storage temperature will be available approximately June 2025.
Product currently supplied and in circulation labelled with storage below 25°C is still appropriate to use.
New Zealand Consumer Medicine Information
Please Note: The storage temperature for Alburex® 5 NZ has been updated to storage below 30°C. Product labelled with the updated storage temperature will be available approximately June 2025.
Product currently supplied and in circulation labelled with storage below 25°C is still appropriate to use.
New Zealand Consumer Medicine Information
Please Note: The storage temperature for Alburex® 20 NZ has been updated to storage below 30°C. Product labelled with the updated storage temperature will be available approximately February 2025.
Product currently supplied and in circulation labelled with storage below 25°C is still appropriate to use.
Australia Consumer Medicine Information
New Zealand Consumer Medicine Information
Andembry® (garadacimab) is currently being evaluated by Pharmac for listing on the Pharmaceutical Schedule.
Australia Consumer Medicine Information
Please Note: An update has been made to remove the plaster from the administration kit for Berinert® IV.
Product supplied without the plaster will be from approximately:
500 IU – June/July 2025
1500 IU – late May/June 2025
Product supplied and in circulation with the plaster in the administration kit is still appropriate to use.
Australia Consumer Medicine Information
Please Note: An update has been made to remove the plaster from the administration kit for Berinert® SC.
Product supplied without the plaster will be from approximately:
2000 IU – late May/June 2025
3000 IU – September/October 2025
Product supplied and in circulation with the plaster in the administration kit is still appropriate to use.
The trademarks marked ® are registered by CSL Limited or its affiliates or subsidiaries in one or more jurisdictions, unless indicated otherwise.

Report an undesirable effect
If you have encountered any side effect(s) to a CSL Behring product, we encourage you to talk to your doctor, pharmacist, or nurse.
CSL Behring also collects information about undesirable effects in order to monitor product safety and investigate, evaluate and report undesirable effects to appropriate regulatory bodies.
Please click on the following link to report an Adverse Event/Undesirable Effect to a CSL Behring product.


