الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
kesimpta
novartis ireland ltd - ofatumumab - heila-og mænusigg, köstum tilkynnt - immunosuppressant - kesimpta is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features (see section 5.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
ozawade
bioprojet pharma - pitolisant - sleep apnea, obstructive - Önnur lyf í taugakerfinu - ozawade is indicated to improve wakefulness and reduce excessive daytime sleepiness (eds) in adult patients with obstructive sleep apnoea (osa).
أيسلندا -
الأيسلاندية -
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
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
vigamox (moxifloxacin alcon) augndropar, lausn 5 mg/ml
novartis healthcare a/s - moxifloxacinum hýdróklóríð - augndropar, lausn - 5 mg/ml
أيسلندا -
الأيسلاندية -
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
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
pramipexole alvogen (vasiprex) tafla 0,18 mg
alvogen ehf. - pramipexolum díhýdróklóríð - tafla - 0,18 mg
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
pramipexole alvogen (vasiprex) tafla 0,088 mg
alvogen ehf. - pramipexolum díhýdróklóríð - tafla - 0,088 mg
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
medikinet cr (medikinet retard) hart hylki með breyttan losunarhraða 30 mg
medice arzneimittel pütter gmbh & co. kg* - methylphenidatum hýdróklóríð - hart hylki með breyttan losunarhraða - 30 mg
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
atomoxetin actavis hart hylki 10 mg
actavis group ptc ehf. - atomoxetinum hýdróklóríð - hart hylki - 10 mg
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
atomoxetin actavis hart hylki 18 mg
actavis group ptc ehf. - atomoxetinum hýdróklóríð - hart hylki - 18 mg