Approvals/TGA/OXYCODONE SANDOZ oxycodone hydrochloride 5 mg modified release tablet blister pack

Approved

STANDARD

OXYCODONE SANDOZ oxycodone hydrochloride 5 mg modified release tablet blister pack

Sandoz Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 28e783a5b6e8dff1
Product Name: OXYCODONE SANDOZ oxycodone hydrochloride 5 mg modified release tablet blister pack
Artg Id: 153605
Artg Name: OXYCODONE SANDOZ oxycodone hydrochloride 5 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: https://medical-cdn.nocode.com/drug_tga/37fdb9431960e73994d1b4115f24e15f.pdf
Product Information: https://medical-cdn.nocode.com/drug_tga/e2a9aa482f7ec3b38519422adeace75d.pdf

Approved

Agency

TGA

Country

🇦🇺

Approval Date

Dec 9, 2025

Approval ID

28e783a5b6e8dff1

Type

Standard