Approvals/TGA/TIXOL 30 duloxetine (as hydrochloride) 30 mg enteric capsule blister pack

Approved

STANDARD

TIXOL 30 duloxetine (as hydrochloride) 30 mg enteric capsule blister pack

Alphapharm Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 031c86df315ee78b
Product Name: TIXOL 30 duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Artg Id: 428623
Artg Name: TIXOL 30 duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Sponsor: Alphapharm Pty Ltd
Company Detail Path: /organization/alphapharm-pty-ltd
Artg Date: 2024-07-15
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/0af898da20f48e6979731ec21ad0b7eb.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/72e403006787b22d86fe5587832e7072.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

031c86df315ee78b

Type

Standard