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ZIPEXOLE pramipexole dihydrochloride 0.25 mg tablets blister pack - TGA Drug Approval Details
Approvals
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TGA
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ZIPEXOLE pramipexole dihydrochloride 0.25 mg tablets blister pack
Approved
STANDARD
ZIPEXOLE pramipexole dihydrochloride 0.25 mg tablets blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 29, 2025
Approval ID
d958a1bc697dc8f3
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
d958a1bc697dc8f3
Product Name
ZIPEXOLE pramipexole dihydrochloride 0.25 mg tablets blister pack
Artg Id
214448
Artg Name
ZIPEXOLE pramipexole dihydrochloride 0.25 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 29, 2025
Approval ID
d958a1bc697dc8f3
Type
Standard
Back to TGA Approvals
