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HUMIRA adalimumab (rch) 20 mg/0.2 mL solution for injection pre- filled syringe - TGA Drug Approval Details
Approvals
/
TGA
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HUMIRA adalimumab (rch) 20 mg/0.2 mL solution for injection pre- filled syringe
Approved
STANDARD
HUMIRA adalimumab (rch) 20 mg/0.2 mL solution for injection pre- filled syringe
AbbVie Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
8540ddd03ff2b026
Company
AbbVie Pty Ltd
Type
Standard
Approval Details
Approval Id
8540ddd03ff2b026
Product Name
HUMIRA adalimumab (rch) 20 mg/0.2 mL solution for injection pre- filled syringe
Artg Id
289104
Artg Name
HUMIRA adalimumab (rch) 20 mg/0.2 mL solution for injection pre-filled syringe
Sponsor
AbbVie Pty Ltd
Company Detail Path
/organization/abbvie-pty-ltd
Artg Date
2018-02-28
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/96c9e7fb0cab00b75b52c5656dd7e3ec.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/d99697291a8f3626839f543c084b2098.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
8540ddd03ff2b026
Type
Standard
Back to TGA Approvals