Approvals/TGA/OXYCODONE SANDOZ oxycodone hydrochloride 20 mg modified release tablet blister pack

Approved

STANDARD

OXYCODONE SANDOZ oxycodone hydrochloride 20 mg modified release tablet blister pack

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: be0f7cb0f43b34ae
Product Name: OXYCODONE SANDOZ oxycodone hydrochloride 20 mg modified release tablet blister pack
Artg Id: 153615
Artg Name: OXYCODONE SANDOZ oxycodone hydrochloride 20 mg modified release tablet blister pack
Sponsor: Sandoz Pty Ltd
Company Detail Path: /organization/sandoz-pty-ltd
Artg Date: 2010-01-20
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2015-CMI-02700-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2010-PI-02329-3

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

be0f7cb0f43b34ae

Type

Standard