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ZIPEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack - TGA Drug Approval Details
Approvals
/
TGA
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ZIPEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Approved
STANDARD
ZIPEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
65e4e84cc60ca500
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
65e4e84cc60ca500
Product Name
ZIPEXOLE pramipexole dihydrochloride 0.125 mg tablets blister pack
Artg Id
214447
Artg Name
ZIPEXOLE 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
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
65e4e84cc60ca500
Type
Standard
Back to TGA Approvals
