Approvals/TGA/PEXEMIS pramipexole dihydrochloride monohydrate 0.5 mg tablet blister pack

Approved

STANDARD

PEXEMIS pramipexole dihydrochloride monohydrate 0.5 mg tablet blister pack

Southern Cross Pharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 6b8050a264b2ff2c
Product Name: PEXEMIS pramipexole dihydrochloride monohydrate 0.5 mg tablet blister pack
Artg Id: 172025
Artg Name: PEXEMIS pramipexole dihydrochloride monohydrate 0.5 mg tablet blister pack
Sponsor: Southern Cross Pharma Pty Ltd
Company Detail Path: /organization/southern-cross-pharma-pty-ltd
Artg Date: 2011-10-25
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

6b8050a264b2ff2c

Type

Standard