Approvals/TGA/PEXEMIS pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack

Approved

STANDARD

PEXEMIS pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack

Southern Cross Pharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: f83ad954605cdc97
Product Name: PEXEMIS pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack
Artg Id: 172024
Artg Name: PEXEMIS pramipexole dihydrochloride monohydrate 0.25 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

Dec 9, 2025

Approval ID

f83ad954605cdc97

Type

Standard