en

PRODUCT DETAIL

Exelon 9,5 mg/24 h transdermálna náplasť

Code 0618B
MA number EU/1/98/066/033
Product Form: emp tdm 42x9,5 mg/24 hodín (vre.pap.PET/Al/PAN)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Novartis Europharm Limited, Ireland
Therapeutic Class: 06 - PSYCHOSTIMULANTIA (NOOTROPNE LIEČ., ANALEPTIKA)
ATC:
N NERVOUS SYSTEM
N06 PSYCHOANALEPTICS
N06D ANTI-DEMENTIA DRUGS
N06DA Anticholinesterases
N06DA03 Rivastigmine
Shelf life: 24
Route of admin.: Transdermal use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application
MA issued: 12.05.1998
SmPC + PL: European Medicines Agency's database
Dokument: Exelon_TTS_DHPC.pdf  
Dokument: Exelon_Pacientsky_dennik.pdf  
Safety feature Yes
Data update: 27.01.2022
eu-flag.png sk-flag.png