Approvals/TGA/SCEMBLIX asciminib (as hydrochloride) 20 mg film-coated tablet blister pack

Approved

STANDARD

SCEMBLIX asciminib (as hydrochloride) 20 mg film-coated tablet blister pack

Approval Id: 703efc901ff226dd
Product Name: SCEMBLIX asciminib (as hydrochloride) 20 mg film-coated tablet blister pack
Artg Id: 371019
Artg Name: SCEMBLIX asciminib (as hydrochloride) 20 mg film-coated tablet blister pack
Sponsor: Novartis Pharmaceuticals Australia Pty Ltd
Company Detail Path: /organization/novartis-pharmaceuticals-australia-pty-ltd
Artg Date: 2022-07-15
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/6dc0b9305193900a9856870057f7fd34.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/fce5054de19e5e97ec5d0591c2ae16cd.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

703efc901ff226dd

Type

Standard