Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
dimethyl fumarate neuraxpharm
laboratorios lesvi s.l. - dímetýl fúmarat - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
dimethyl fumarate mylan
mylan ireland limited - dímetýl fúmarat - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
dimethyl fumarate polpharma
zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dímetýl fúmarat - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
dimethyl fumarate teva
teva gmbh - dímetýl fúmarat - multiple sclerosis, relapsing-remitting; multiple sclerosis - Ónæmisbælandi lyf - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
dimethyl fumarate accord
accord healthcare s.l.u. - dímetýl fúmarat - multiple sclerosis, relapsing-remitting; multiple sclerosis - Ónæmisbælandi lyf - dimethyl fumarate accord is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
methylphenidate stada hart hylki með breyttan losunarhraða 30 mg
stada arzneimittel ag - methylphenidatum hýdróklóríð - hart hylki með breyttan losunarhraða - 30 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
methylphenidate stada hart hylki með breyttan losunarhraða 20 mg
stada arzneimittel ag - methylphenidatum hýdróklóríð; methylphenidatum hýdróklóríð - hart hylki með breyttan losunarhraða - 20 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
methylphenidate stada hart hylki með breyttan losunarhraða 40 mg
stada arzneimittel ag - methylphenidatum hýdróklóríð - hart hylki með breyttan losunarhraða - 40 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
methylphenidate stada hart hylki með breyttan losunarhraða 60 mg
stada arzneimittel ag - methylphenidatum hýdróklóríð - hart hylki með breyttan losunarhraða - 60 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
methylphenidate sandoz forðatafla 54 mg
sandoz a/s* - methylphenidatum hýdróklóríð - forðatafla - 54 mg