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REMINYL galantamine 16mg (as hydrobromide) modified release capsule - TGA Drug Approval Details
Approvals
/
TGA
/
REMINYL galantamine 16mg (as hydrobromide) modified release capsule
Approved
STANDARD
REMINYL galantamine 16mg (as hydrobromide) modified release capsule
Clinect Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
34709e2fedad2466
Company
Clinect Pty Ltd
Type
Standard
Approval Details
Approval Id
34709e2fedad2466
Product Name
REMINYL galantamine 16mg (as hydrobromide) modified release capsule
Artg Id
97885
Artg Name
REMINYL galantamine 16mg (as hydrobromide) modified release capsule blister pack
Sponsor
Clinect Pty Ltd
Company Detail Path
/organization/clinect-pty-ltd
Artg Date
2004-05-19
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/c728232c3eb55ef5e20ebc7b79fa0ddb.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/487f691b9367b88ed390be3567d93d92.pdf
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
34709e2fedad2466
Type
Standard
Back to TGA Approvals