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DULOXETINE AN duloxetine 60 mg (as hydrochloride) enteric capsule bottle - TGA Drug Approval Details
Approvals
/
TGA
/
DULOXETINE AN duloxetine 60 mg (as hydrochloride) enteric capsule bottle
Approved
STANDARD
DULOXETINE AN duloxetine 60 mg (as hydrochloride) enteric capsule bottle
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
bdce49511ddde46e
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
bdce49511ddde46e
Product Name
DULOXETINE AN duloxetine 60 mg (as hydrochloride) enteric capsule bottle
Artg Id
199001
Artg Name
DULOXETINE AN duloxetine 60 mg (as hydrochloride) enteric capsule bottle
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2013-07-01
Registration Type
Medicine
Therapeutic Good Type
Medicine
Licence Status
A
Licence Category
RE
Product Information
https://medical-cdn.nocode.com/drug_tga/b1f5ba36239832daeb3c4ea4b3e320d8.pdf
Active Ingredients
Approved
Quick Info
Agency
TGA
Country
🇦🇺
Approval Date
May 30, 2025
Approval ID
bdce49511ddde46e
Type
Standard
Back to TGA Approvals
