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DULOXETINE DR-LUPIN duloxetine (as hydrochloride) 30mg capsules blister pack - TGA Drug Approval Details
Approvals
/
TGA
/
DULOXETINE DR-LUPIN duloxetine (as hydrochloride) 30mg capsules blister pack
Approved
STANDARD
DULOXETINE DR-LUPIN duloxetine (as hydrochloride) 30mg capsules blister pack
Lupin Australia Pty Limited
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
803a5213da0771b6
Company
Lupin Australia Pty Limited
Type
Standard
Approval Details
Approval Id
803a5213da0771b6
Product Name
DULOXETINE DR-LUPIN duloxetine (as hydrochloride) 30mg capsules blister pack
Artg Id
197162
Artg Name
DULOXETINE DR-LUPIN duloxetine (as hydrochloride) 30mg enteric capsules blister pack
Sponsor
Lupin Australia Pty Limited
Company Detail Path
/organization/lupin-australia-pty-limited
Artg Date
2013-04-29
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Consumer Medicine Info
https://medical-cdn.nocode.com/drug_tga/8300df6aa60f573a6cedb39d1d3c2a42.pdf
Product Information
https://medical-cdn.nocode.com/drug_tga/ec963d39a5e276ef14631eade61f7290.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
803a5213da0771b6
Type
Standard
Back to TGA Approvals