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FLUOXETINE GENERICHEALTH fluoxetine (as hydrochloride) 20 mg capsule blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
FLUOXETINE GENERICHEALTH fluoxetine (as hydrochloride) 20 mg capsule blister pack
Approved
STANDARD
FLUOXETINE GENERICHEALTH fluoxetine (as hydrochloride) 20 mg capsule blister pack
Generic Health Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
1edb9c090a6ea0bc
Company
Generic Health Pty Ltd
Type
Standard
Approval Details
Approval Id
1edb9c090a6ea0bc
Product Name
FLUOXETINE GENERICHEALTH fluoxetine (as hydrochloride) 20 mg capsule blister pack
Artg Id
146600
Artg Name
FLUOXETINE GENERICHEALTH fluoxetine (as hydrochloride) 20 mg capsule blister pack
Sponsor
Generic Health Pty Ltd
Company Detail Path
/organization/generic-health-pty-ltd
Artg Date
2008-10-21
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/02a637b723c2a4ab33eeb5883bebe9b5.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/b7af2e8817d25450ca7a86caa0ebebc5.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
1edb9c090a6ea0bc
Type
Standard
Back to TGA Approvals