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REMINYL galantamine 24mg (as hydrobromide) modified release capsule - TGA Drug Approval Details
Approvals
/
TGA
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REMINYL galantamine 24mg (as hydrobromide) modified release capsule
Approved
STANDARD
REMINYL galantamine 24mg (as hydrobromide) modified release capsule
Clinect Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
e536dd7e2a40aff1
Company
Clinect Pty Ltd
Type
Standard
Approval Details
Approval Id
e536dd7e2a40aff1
Product Name
REMINYL galantamine 24mg (as hydrobromide) modified release capsule
Artg Id
97887
Artg Name
REMINYL galantamine 24mg (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
http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-CMI-04280-3
Product Information
http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-PI-04279-3
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
e536dd7e2a40aff1
Type
Standard
Back to TGA Approvals