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OXYNALGIN 5/2.5 oxycodone hydrochloride 5mg naloxone hydrochloride 2.5mg modified release tablet blister - TGA Drug Approval Details
Approvals
/
TGA
/
OXYNALGIN 5/2.5 oxycodone hydrochloride 5mg naloxone hydrochloride 2.5mg modified release tablet blister
Approved
STANDARD
OXYNALGIN 5/2.5 oxycodone hydrochloride 5mg naloxone hydrochloride 2.5mg modified release tablet blister
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
6f98b34bc3866884
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
6f98b34bc3866884
Product Name
OXYNALGIN 5/2.5 oxycodone hydrochloride 5mg naloxone hydrochloride 2.5mg modified release tablet blister
Artg Id
330691
Artg Name
OXYNALGIN 5/2.5 oxycodone hydrochloride 5mg naloxone hydrochloride 2.5mg modified release tablet blister
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2024-07-03
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
6f98b34bc3866884
Type
Standard
Back to TGA Approvals