Approvals/TGA/ARX-Oxycodone/Naloxone oxycodone hydrochloride / naloxone hydrochloride 60/30 mg modified release tablets blister pack

Approved

STANDARD

ARX-Oxycodone/Naloxone oxycodone hydrochloride / naloxone hydrochloride 60/30 mg modified release tablets blister pack

Mundipharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 32d17eff9109d1e1
Product Name: ARX-Oxycodone/Naloxone oxycodone hydrochloride / naloxone hydrochloride 60/30 mg modified release tablets blister pack
Artg Id: 446612
Artg Name: ARX-Oxycodone/Naloxone oxycodone hydrochloride / naloxone hydrochloride 60/30 mg modified release tablets blister pack
Sponsor: Mundipharma Pty Ltd
Company Detail Path: /organization/mundipharma-pty-ltd
Artg Date: 2024-10-08
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: https://medical-cdn.nocode.com/drug_tga/7cb7f0a386c921c206e1747384c3e458.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/c307e3c940b8b173594be2262c9dd30f.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

32d17eff9109d1e1

Type

Standard