Aspen Pharma Pty Ltd — Endone Oxycodone Hydrochloride 5mg Tablet Blister Pack

PRA number


Published date

Product description

Endone oxycodone hydrochloride 5mg tablet blister pack
Batch Number: CW612
Expiry: Nov 2020

AUST R: 14945
Photograph of Endone and Anamorph Blister Sheets
Identifying features

Other identifying numbers

Batch Number CW612

Reasons the product is recalled

A report has been received that a strip of 30mg Anamorph tablets may have been present in a box of 5mg Endone, post dispensing.

The hazards to consumers

Anamorph tablets are approximately four times the Endone equivalent dose, so there is the potential of serious health risks and overdose, if taken inadvertently.

What consumers should do

Consumers should visually inspect blister sheets to verify both blister strips contain Endone tablets. If a blister is identified with Anamorph printed on the back, do not use the tablets from that strip. Return strips of incorrect tablets to the chemist or pharmacy from which they were purchased.

Further information is available on the TGA website at:

For further information, contact Aspen Pharma by phone on 1300 659 646 or email at

Traders who sold this product

Pharmacies and Chemists

Where the product was sold


Responsible regulator

Therapeutic Goods Administration is the responsible regulator for this recall.

Product category