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GALANTYL galantamine (as hydrobromide) 8 mg modified release capsule blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
GALANTYL galantamine (as hydrobromide) 8 mg modified release capsule blister pack
Approved
STANDARD
GALANTYL galantamine (as hydrobromide) 8 mg modified release capsule blister pack
Alphapharm Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 29, 2025
Approval ID
9c998fe3d259d01e
Company
Alphapharm Pty Ltd
Type
Standard
Approval Details
Approval Id
9c998fe3d259d01e
Product Name
GALANTYL galantamine (as hydrobromide) 8 mg modified release capsule blister pack
Artg Id
157934
Artg Name
GALANTYL galantamine (as hydrobromide) 8 mg modified release capsule blister pack
Sponsor
Alphapharm Pty Ltd
Company Detail Path
/organization/alphapharm-pty-ltd
Artg Date
2010-04-23
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/2bcc19a45494a3dfc71a53103b7ad02a.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/abf46c464b8e64d65236f526233e0bd4.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 29, 2025
Approval ID
9c998fe3d259d01e
Type
Standard
Back to TGA Approvals