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PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Approved
STANDARD
PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
dae07793e59f1b06
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
dae07793e59f1b06
Product Name
PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Artg Id
214442
Artg Name
PEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2014-09-23
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
dae07793e59f1b06
Type
Standard
Back to TGA Approvals