Skip to main content

XEMBIFY (Grifols Australia Pty Ltd)

Product name
XEMBIFY
Date registered
Evaluation commenced
Decision date
Approval time
143 (255 working days)
Active ingredients
human immunoglobulin G
Registration type
NCE/NBE
Indication

Indications for subcutaneous administration (SCIg)

XEMBIFY (solution for subcutaneous injection) is indicated as replacement therapy in adult and paediatric patients for:

  • Primary immunodeficiency diseases (PID)
  • Symptomatic hypogammaglobulinaemia secondary to underlying disease or treatment.
  • Help us improve the Therapeutic Goods Administration site