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APO-FLUOXETINE 20mg fluoxetine (as hydrochloride) 20 mg capsules blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
APO-FLUOXETINE 20mg fluoxetine (as hydrochloride) 20 mg capsules blister pack
Approved
STANDARD
APO-FLUOXETINE 20mg fluoxetine (as hydrochloride) 20 mg capsules blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
6e2026db73ff48bc
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
6e2026db73ff48bc
Product Name
APO-FLUOXETINE 20mg fluoxetine (as hydrochloride) 20 mg capsules blister pack
Artg Id
273924
Artg Name
APO-FLUOXETINE 20mg fluoxetine (as hydrochloride) 20 mg capsules blister pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2017-02-23
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/2a38c17ba98858eaeb92ad5893380c18.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/2818d0f0f7657e68bf0264c901f62471.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
6e2026db73ff48bc
Type
Standard
Back to TGA Approvals