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PRODUCT DETAIL

Myfenax 500 mg filmom obalené tablety

Code 2125A
MA number EU/1/07/438/005
Product Form: tbl flm 50x1x500 mg (blis.PVC/PVDC/Al - jednotk.bal.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L04 Immunosuppressants
L04A Immunosuppressants
L04AA Selective immunosuppressants
L04AA06 Mycophenolic acid
Shelf life: 36
Container: blister PVC/PVDC/Al
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 21.02.2008
SmPC + PL: European Medicines Agency's database
Dokument: DHPC mykofenolat 3 12 2015.pdf  
Safety feature Yes
Data update: 11.07.2023
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