Approvals/TGA/PEXEMIS pramipexole dihydrochloride monohydrate 0.125 mg tablet blister pack

Approved

STANDARD

PEXEMIS pramipexole dihydrochloride monohydrate 0.125 mg tablet blister pack

Southern Cross Pharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: b1bf32da31dbed42
Product Name: PEXEMIS pramipexole dihydrochloride monohydrate 0.125 mg tablet blister pack
Artg Id: 172023
Artg Name: PEXEMIS pramipexole dihydrochloride monohydrate 0.125 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

b1bf32da31dbed42

Type

Standard