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PRODUCT DETAIL

Peyona 20 mg/ml infúzny intravenózny roztok a perorálny roztok

Code 07849
MA number EU/1/09/528/002
Product Form: sol ipr 10x1 ml/20 mg (amp.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 06 - PSYCHOSTIMULANTIA (NOOTROPNE LIEČ., ANALEPTIKA)
ATC:
N NERVOUS SYSTEM
N06 PSYCHOANALEPTICS
N06B PSYCHOSTIMULANTS AND NOOTROPICS
N06BC Xanthine derivatives
N06BC01 Caffeine
Shelf life: 36
Container: glass ampoule
Route of admin.: Intravenous and oromucosal use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10a well-established use application
MA issued: 04.06.2010
SmPC + PL: European Medicines Agency's database
Dokument: DHPC Peyona kofeín 30-11-2011.pdf  
Safety feature Yes
Data update: 21.06.2022
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