Approvals/TGA/LURASIDONE SANDOZ lurasidone hydrochloride 80 mg film-coated tablet blister pack

Approved

STANDARD

LURASIDONE SANDOZ lurasidone hydrochloride 80 mg film-coated tablet blister pack

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: f7a5d78bab8481ca
Product Name: LURASIDONE SANDOZ lurasidone hydrochloride 80 mg film-coated tablet blister pack
Artg Id: 321689
Artg Name: LURASIDONE SANDOZ lurasidone hydrochloride 80 mg film-coated tablet blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2020-06-24
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/bc8863eaacb2801e0170dab89545fafb.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/2953fd08e36c0b962b90622de6820520.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

f7a5d78bab8481ca

Type

Standard