Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
ganirelix gedeon richter
chemical works of gedeon richter plc. (gedeon richter plc.) - ganirelix acetate - reproductive techniques, assisted; ovulation induction; infertility, female - hinsveiflur og heilahimnubólur og hliðstæður - prevention of premature luteinising hormone (lh) surges in women undergoing controlled ovarian hyperstimulation (coh) for assisted reproduction techniques (art).
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
phosphoral mixtúra, lausn 24,4 g/10,8 g
casen recordati s.l. - dinatrii hydrogenophosphas; natrii dihydrogenophosphas - mixtúra, lausn - 24,4 g/10,8 g
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
hemangiol
pierre fabre medicament - própranólól hýdróklóríð - hemangioma - betablokkar - hemangiol is indicated in the treatment of proliferating infantile haemangioma requiring systemic therapy: , life- or function-threatening haemangioma,, ulcerated haemangioma with pain and/or lack of response to simple wound care measures,, haemangioma with a risk of permanent scars or disfigurement. , it is to be initiated in infants aged 5 weeks to 5 months.
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
atomoxetine stada hart hylki 60 mg
stada arzneimittel ag - atomoxetinum hýdróklóríð - hart hylki - 60 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
atomoxetine stada hart hylki 40 mg
stada arzneimittel ag - atomoxetinum hýdróklóríð - hart hylki - 40 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
atomoxetine stada hart hylki 10 mg
stada arzneimittel ag - atomoxetinum hýdróklóríð - hart hylki - 10 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
atomoxetine stada hart hylki 18 mg
stada arzneimittel ag - atomoxetinum hýdróklóríð - hart hylki - 18 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
atomoxetine stada hart hylki 25 mg
stada arzneimittel ag - atomoxetinum hýdróklóríð - hart hylki - 25 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
atomoxetine stada hart hylki 80 mg
stada arzneimittel ag - atomoxetinum hýdróklóríð - hart hylki - 80 mg
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
ellaone
laboratoire hra pharma - ulipristal - getnaðarvörn, postcoital - hormón kynlíf og stillum á kynfærum kerfi, , neyðarástand getnaðarvarna - neyðartilvikum getnaðarvörn innan 120 klukkustundir (fimm daga) varnarlausa samfarir eða getnaðarvörn bilun.