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TEXOTINE duloxetine (as hydrochloride) 30 mg enteric capsule bottle - TGA Drug Approval Details
Approvals
/
TGA
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TEXOTINE duloxetine (as hydrochloride) 30 mg enteric capsule bottle
Approved
STANDARD
TEXOTINE duloxetine (as hydrochloride) 30 mg enteric capsule bottle
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
8b56a9fcf63286cc
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
8b56a9fcf63286cc
Product Name
TEXOTINE duloxetine (as hydrochloride) 30 mg enteric capsule bottle
Artg Id
289483
Artg Name
TEXOTINE 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
8b56a9fcf63286cc
Type
Standard
Back to TGA Approvals
