Approvals/TGA/MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 60/30 mg modified release tablet blister pack

Approved

STANDARD

MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 60/30 mg modified release tablet blister pack

Mundipharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: cfd2d082884d6732
Product Name: MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 60/30 mg modified release tablet blister pack
Artg Id: 288271
Artg Name: MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 60/30 mg modified release tablet blister pack
Sponsor: Mundipharma Pty Ltd
Company Detail Path: /organization/mundipharma-pty-ltd
Artg Date: 2022-10-17
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

cfd2d082884d6732

Type

Standard