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PRODUCT DETAIL

Relistor 12 mg/0,6 ml injekčný roztok

Code 51896
MA number EU/1/08/463/002
Product Form: sol inj 2x0,6 ml/12 mg (2 liek.inj.skl.+2 steril.inj.striek.+4 alkoh.tamp.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 87 - VARIA I
ATC:
A ALIMENTARY TRACT AND METABOLISM
A06 DRUGS FOR CONSTIPATION
A06A DRUGS FOR CONSTIPATION
A06AH Peripheral opioid receptor antagonists
A06AH01 Methylnatrexone bromide
Shelf life: 48
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 02.07.2008
SmPC + PL: European Medicines Agency's database
Dokument: Relistor DHCP 06 09 2010.pdf  
Safety feature Yes
Data update: 29.04.2024
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