OxyContin 40 mg prolonged release tablets

Licence status
Authorised: 28/05/1998
Active substances
OXYCODONE HYDROCHLORIDE
Dosage Form
Prolonged-release tablet
Licence number
PA1688/005/004
Licence holder
Mundipharma Pharmaceuticals Limited

Product documents

Licence information

ATC code
N02AA Natural opium alkaloids, N02AA05 oxycodone
Legal supply status
Product subject to prescription which may not be renewed (A)
Place of sale
Supply through pharmacies only
Conditions of Licence
This product contains a substance listed in schedule 2 to the Misuse of Drugs Regulations 2017.
Marketing availability
Marketed
Advertising conditions
Advertising to healthcare professionals only
Licence issued
28/05/1998

Interchangeable information