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GXP OXYCODONE oxycodone hydrochloride 5mg film coated tablet blister pack - TGA Drug Approval Details
Approvals
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TGA
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GXP OXYCODONE oxycodone hydrochloride 5mg film coated tablet blister pack
Approved
STANDARD
GXP OXYCODONE oxycodone hydrochloride 5mg film coated tablet blister pack
Arrotex Pharmaceuticals Pty Ltd
🇦🇺 Therapeutic Goods Administration
Approval Date
May 30, 2025
Approval ID
8bf769fac1a2c682
Company
Arrotex Pharmaceuticals Pty Ltd
Type
Standard
Approval Details
Approval Id
8bf769fac1a2c682
Product Name
GXP OXYCODONE oxycodone hydrochloride 5mg film coated tablet blister pack
Artg Id
297746
Artg Name
GXP OXYCODONE oxycodone hydrochloride 5mg film coated tablet blister pack
Sponsor
Arrotex Pharmaceuticals Pty Ltd
Company Detail Path
/organization/arrotex-pharmaceuticals-pty-ltd
Artg Date
2019-05-29
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
8bf769fac1a2c682
Type
Standard
Back to TGA Approvals
