Approvals/TGA/APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 1 mg tablet blister pack

Approved

STANDARD

APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 1 mg tablet blister pack

Southern Cross Pharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: d6c999e4a995a9a3
Product Name: APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 1 mg tablet blister pack
Artg Id: 227669
Artg Name: APO-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 1 mg tablet blister pack
Sponsor: Southern Cross Pharma Pty Ltd
Company Detail Path: /organization/southern-cross-pharma-pty-ltd
Artg Date: 2015-11-17
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/91952c063bf95041eec0aee12da5f438.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/dd852559af8dd0a929c28c0285ef6599.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

d6c999e4a995a9a3

Type

Standard