Approvals/TGA/PAROXETINE SANDOZ paroxetine (as hydrochloride) 20mg tablet blister pack

Approved

STANDARD

PAROXETINE SANDOZ paroxetine (as hydrochloride) 20mg tablet blister pack

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 3b95f3c9a8e307d2
Product Name: PAROXETINE SANDOZ paroxetine (as hydrochloride) 20mg tablet blister pack
Artg Id: 82551
Artg Name: PAROXETINE SANDOZ paroxetine (as hydrochloride) 20mg tablet blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2002-05-09
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/7c2c2aa0aca5d77bdc728cb15c4f9593.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/f4047addf66a95d9c500f32c7c480918.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

3b95f3c9a8e307d2

Type

Standard