OXYCODONE SANDOZ oxycodone hydrochloride 5 mg modified release tablet blister pack, Sandoz Pty Ltd , CON-1465
Product name
OXYCODONE SANDOZ oxycodone hydrochloride 5 mg modified release tablet blister pack
Sponsor name
Sandoz Pty Ltd
Batches
PS9028
Consent start
Consent no.
CON-1465
Duration
The consent is effective from 12 February 2026 until 12 February 2027.
Standard
Subparagraph 10(14)(a)(iv) of Therapeutic Goods Order No. 91 - Standard for labels of prescription and related medicines
Non-compliance with standard
The approved name of the medicine is ‘OXYCODONE SANDOZ oxycodone hydrochloride 5
mg modified release tablet’ whilst the name on the blister pack is included as
‘OXYCODONE SANDOZ oxycodone hydrochloride 5 mg tablet’.
Conditions imposed
A ‘Dear Healthcare Provider’ letter will be supplied with each affected batch.
It will remind users to leave the blister strip in the original carton.
Import, Supply, &/or Export
import and supply
Therapeutic product type
Prescription medicines