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Armoneve 20 mg/10 mg prolonged-release tablets

20/10 mg/mg Prolonged-release tablet

Mundipharma Pharmaceuticals LimitedPA1688/017/005

Main Information

Trade NameArmoneve 20 mg/10 mg prolonged-release tablets
Active SubstancesOXYCODONE HYDROCHLORIDE
Naloxone hydrochloride dihydrate
Strength20/10 mg/mg
Dosage FormProlonged-release tablet
Licence HolderMundipharma Pharmaceuticals Limited
Licence NumberPA1688/017/005

Group Information

ATC CodeN02AA Natural opium alkaloids
N02AA55 oxycodone, combinations

Status

Authorised/WithdrawnWithdrawn
Withdrawn Date29/10/2019
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of LicenceThis product contains a substance listed in schedule 2 to the Misuse of Drugs Regulations 2017.
Marketing StatusNot marketed

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportNo document available

Generics Information

Interchangeable List CodeIC0102-061-024
Interchangeable List DocumentPDF of Interchangeable List
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