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APO-Duloxetine duloxetine (as hydrochloride) 60 mg enteric capsule bottle - TGA Drug Approval Details
Approvals
/
TGA
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APO-Duloxetine duloxetine (as hydrochloride) 60 mg enteric capsule bottle
Approved
STANDARD
APO-Duloxetine duloxetine (as hydrochloride) 60 mg enteric capsule bottle
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
94d22d55fcbe1d5f
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
94d22d55fcbe1d5f
Product Name
APO-Duloxetine duloxetine (as hydrochloride) 60 mg enteric capsule bottle
Artg Id
195362
Artg Name
APO-DULOXETINE duloxetine (as hydrochloride) 60 mg enteric capsule bottle pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2012-11-30
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
94d22d55fcbe1d5f
Type
Standard
Back to TGA Approvals
