Approvals/TGA/HUMIRA adalimumab 80 mg/0.8 mL injection solution pre-filled syringe

Approved

STANDARD

HUMIRA adalimumab 80 mg/0.8 mL injection solution pre-filled syringe

AbbVie Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 8a54a5ecda727960
Product Name: HUMIRA adalimumab 80 mg/0.8 mL injection solution pre-filled syringe
Artg Id: 292934
Artg Name: HUMIRA adalimumab 80 mg/0.8 mL injection solution pre-filled syringe
Sponsor: AbbVie Pty Ltd
Company Detail Path: /organization/abbvie-pty-ltd
Artg Date: 2018-01-03
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-2021-CMI-01077-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-PI-03779-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

8a54a5ecda727960

Type

Standard