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PRAMIPEX XR pramipexole dihydrochloride monohydrate 3 mg modified release tablet blister pack
Approved
STANDARD
PRAMIPEX XR pramipexole dihydrochloride monohydrate 3 mg modified release tablet blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
ef6c1e680d57b275
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
ef6c1e680d57b275
Product Name
PRAMIPEX XR pramipexole dihydrochloride monohydrate 3 mg modified release tablet blister pack
Artg Id
225619
Artg Name
PRAMIPEX XR pramipexole dihydrochloride monohydrate 3 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
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
ef6c1e680d57b275
Type
Standard
Back to TGA Approvals
PRAMIPEX XR pramipexole dihydrochloride monohydrate 3 mg modified release tablet blister pack - TGA Drug Approval Details
