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APOTEX-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
APOTEX-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack
Approved
STANDARD
APOTEX-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
af3afe6820f81b91
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
af3afe6820f81b91
Product Name
APOTEX-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack
Artg Id
168558
Artg Name
APOTEX-PRAMIPEXOLE pramipexole dihydrochloride monohydrate 0.25 mg tablet blister pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2011-11-04
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
af3afe6820f81b91
Type
Standard
Back to TGA Approvals
