Approvals/TGA/MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 80/40 mg modified release tablet blister pack

Approved

STANDARD

MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 80/40 mg modified release tablet blister pack

Mundipharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 41cb34e7f48e02ea
Product Name: MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 80/40 mg modified release tablet blister pack
Artg Id: 288272
Artg Name: MPL- OXYCODONE/NALOXONE oxycodone hydrochloride / naloxone hydrochloride 80/40 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

May 30, 2025

Approval ID

41cb34e7f48e02ea

Type

Standard