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DULOXETINE GXP duloxetine (as hydrochloride) 30 mg enteric capsule bottle - TGA Drug Approval Details
Approvals
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TGA
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DULOXETINE GXP duloxetine (as hydrochloride) 30 mg enteric capsule bottle
Approved
STANDARD
DULOXETINE GXP duloxetine (as hydrochloride) 30 mg enteric capsule bottle
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
a8ab100acecd4cbb
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
a8ab100acecd4cbb
Product Name
DULOXETINE GXP duloxetine (as hydrochloride) 30 mg enteric capsule bottle
Artg Id
289468
Artg Name
DULOXETINE GXP duloxetine (as hydrochloride) 30 mg enteric capsule bottle
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
a8ab100acecd4cbb
Type
Standard
Back to TGA Approvals
