Approvals/TGA/LURASIDONE SUN lurasidone hydrochloride 40 mg film-coated tablet blister pack

Approved

STANDARD

LURASIDONE SUN lurasidone hydrochloride 40 mg film-coated tablet blister pack

Sun Pharma ANZ Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: a13fa63cfd6cf11f
Product Name: LURASIDONE SUN lurasidone hydrochloride 40 mg film-coated tablet blister pack
Artg Id: 330268
Artg Name: LURASIDONE SUN lurasidone hydrochloride 40 mg film-coated tablet blister pack
Sponsor: Sun Pharma ANZ Pty Ltd
Company Detail Path: /organization/sun-pharma-anz-pty-ltd
Artg Date: 2020-11-12
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/18069516b0ab5e98297130042fc29701.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/0bcfd80941be53daad22c20854cb833a.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 29, 2025

Approval ID

a13fa63cfd6cf11f

Type

Standard