Approvals/TGA/OXYCONTIN oxycodone hydrochloride 10mg modified release tablet blister pack

Approved

STANDARD

OXYCONTIN oxycodone hydrochloride 10mg modified release tablet blister pack

Mundipharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: f284d5c4344a5252
Product Name: OXYCONTIN oxycodone hydrochloride 10mg modified release tablet blister pack
Artg Id: 200031
Artg Name: OXYCONTIN oxycodone hydrochloride 10mg modified release tablet blister pack
Sponsor: Mundipharma Pty Ltd
Company Detail Path: /organization/mundipharma-pty-ltd
Artg Date: 2013-10-22
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/6f2678d07bda538d9940a9d9ebf5f3b6.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/1c1bcb74b249ce25929efa1f85cccf72.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

f284d5c4344a5252

Type

Standard