Approvals/TGA/ERLOTINIB ARX erlotinib (as hydrochloride) 25 mg film-coated tablet blister pack

Approved

STANDARD

ERLOTINIB ARX erlotinib (as hydrochloride) 25 mg film-coated tablet blister pack

Accelagen Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 55b41f31de032525
Product Name: ERLOTINIB ARX erlotinib (as hydrochloride) 25 mg film-coated tablet blister pack
Artg Id: 324444
Artg Name: ERLOTINIB ARX erlotinib (as hydrochloride) 25 mg film-coated tablet blister pack
Sponsor: Accelagen Pty Ltd
Company Detail Path: /organization/accelagen-pty-ltd
Artg Date: 2020-08-12
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/e612f59127e12fd18953f3d814f97f05.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/e5dc093d1026fa705761e59c1c8d9f29.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

55b41f31de032525

Type

Standard