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DULOXETINE-WGR duloxetine (as hydrochloride) 30 mg enteric capsule blister pack - TGA Drug Approval Details
Approvals
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TGA
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DULOXETINE-WGR duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Approved
STANDARD
DULOXETINE-WGR duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
GM Pharma International Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
Dec 9, 2025
Approval ID
40c0810118b5a2ec
Company
GM Pharma International Pty Ltd
Type
Standard
Approval Details
Approval Id
40c0810118b5a2ec
Product Name
DULOXETINE-WGR duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Artg Id
421534
Artg Name
DULOXETINE-WGR duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Sponsor
GM Pharma International Pty Ltd
Company Detail Path
/organization/gm-pharma-international-pty-ltd
Artg Date
2024-08-13
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
Dec 9, 2025
Approval ID
40c0810118b5a2ec
Type
Standard
Back to TGA Approvals