Armoneve 5 mg / 2.5 mg prolonged-release tablets
- Licence status
- Withdrawn: 29/10/2019
- Active substances
- OXYCODONE HYDROCHLORIDE, Naloxone hydrochloride dihydrate
- Dosage Form
- Prolonged-release tablet
- Licence number
- PA1688/017/002
- Licence holder
- Mundipharma Pharmaceuticals Limited
Product documents
- Package Leaflet
- Summary of Product Characteristics
- Public Assessment Report
Licence information
- ATC code
- N02AA Natural opium alkaloids, N02AA55 oxycodone, combinations
- 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
- Not marketed
- Advertising conditions
- Advertising to healthcare professionals only
- Licence issued
- 05/03/2018