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MIMIVA memantine hydrochloride 10 mg tablet blister pack - TGA Drug Approval Details
Approvals
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TGA
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MIMIVA memantine hydrochloride 10 mg tablet blister pack
Approved
STANDARD
MIMIVA memantine hydrochloride 10 mg tablet blister pack
Sun Pharma ANZ Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
6ccfe5b05f5192ec
Company
Sun Pharma ANZ Pty Ltd
Type
Standard
Approval Details
Approval Id
6ccfe5b05f5192ec
Product Name
MIMIVA memantine hydrochloride 10 mg tablet blister pack
Artg Id
201736
Artg Name
MIMIVA memantine hydrochloride 10 mg tablet blister pack
Sponsor
Sun Pharma ANZ Pty Ltd
Company Detail Path
/organization/sun-pharma-anz-pty-ltd
Artg Date
2013-11-28
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
6ccfe5b05f5192ec
Type
Standard
Back to TGA Approvals
