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DULOXETINE AP duloxetine (as hydrochloride) 30 mg enteric capsule blister pack - TGA Drug Approval Details
Approvals
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TGA
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DULOXETINE AP duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Approved
STANDARD
DULOXETINE AP duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
2fda30a21a67fd1d
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
2fda30a21a67fd1d
Product Name
DULOXETINE AP duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Artg Id
289467
Artg Name
DULOXETINE AP duloxetine (as hydrochloride) 30 mg enteric capsule blister pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2018-07-31
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
2fda30a21a67fd1d
Type
Standard
Back to TGA Approvals
