Approvals/TGA/PEXOLE XR pramipexole dihydrochloride monohydrate 1.5 mg modified release tablet blister pack

Approved

STANDARD

PEXOLE XR pramipexole dihydrochloride monohydrate 1.5 mg modified release tablet blister pack

Arrotex Pharmaceuticals Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 0e1be872fe547dfb
Product Name: PEXOLE XR pramipexole dihydrochloride monohydrate 1.5 mg modified release tablet blister pack
Artg Id: 225581
Artg Name: PEXOLE XR pramipexole dihydrochloride monohydrate 1.5 mg modified release tablet blister pack
Sponsor: Arrotex Pharmaceuticals Pty Ltd
Company Detail Path: /organization/arrotex-pharmaceuticals-pty-ltd
Artg Date: 2015-06-17
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

0e1be872fe547dfb

Type

Standard