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EFEXOR-XR venlafaxine (as hydrochloride) 75mg modified release capsule blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
EFEXOR-XR venlafaxine (as hydrochloride) 75mg modified release capsule blister pack
Approved
STANDARD
EFEXOR-XR venlafaxine (as hydrochloride) 75mg modified release capsule blister pack
Viatris Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
0253dd7b43d79660
Company
Viatris Pty Ltd
Type
Standard
Approval Details
Approval Id
0253dd7b43d79660
Product Name
EFEXOR-XR venlafaxine (as hydrochloride) 75mg modified release capsule blister pack
Artg Id
60858
Artg Name
EFEXOR-XR venlafaxine (as hydrochloride) 75mg modified release capsule blister pack
Sponsor
Viatris Pty Ltd
Company Detail Path
/organization/viatris-pty-ltd
Artg Date
1998-05-11
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/c9fe7eb61bacbebfff237f12c2a4bc45.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/93528e720b87bfdbb9bb5d5539f3624e.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
0253dd7b43d79660
Type
Standard
Back to TGA Approvals