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HIZENTRA human normal immunoglobulin 20% solution for subcutaneous injection 50 mL vial - TGA Drug Approval Details
Approvals
/
TGA
/
HIZENTRA human normal immunoglobulin 20% solution for subcutaneous injection 50 mL vial
Approved
STANDARD
HIZENTRA human normal immunoglobulin 20% solution for subcutaneous injection 50 mL vial
CSL Behring (Australia) Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
a662407b0996a18a
Company
CSL Behring (Australia) Pty Ltd
Type
Standard
Approval Details
Approval Id
a662407b0996a18a
Product Name
HIZENTRA human normal immunoglobulin 20% solution for subcutaneous injection 50 mL vial
Artg Id
207384
Artg Name
HIZENTRA human normal immunoglobulin 20% solution for subcutaneous injection 50 mL vial
Sponsor
CSL Behring (Australia) Pty Ltd
Company Detail Path
/organization/csl-behring-australia-pty-ltd
Artg Date
2014-05-08
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2025-CMI-01242-1
Product Information
http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2014-PI-03180-1
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
a662407b0996a18a
Type
Standard
Back to TGA Approvals