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.
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
omnipaque stungulyf, lausn 350 mg j/ml
ge healthcare as - iohexolum inn - stungulyf, lausn - 350 mg j/ml
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
omnipaque stungulyf, lausn 300 mg j/ml
ge healthcare as - iohexolum inn - stungulyf, lausn - 300 mg j/ml
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
omnipaque stungulyf, lausn 180 mg j/ml
ge healthcare as - iohexolum inn - stungulyf, lausn - 180 mg j/ml
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
omnipaque stungulyf, lausn 140 mg j/ml
ge healthcare as - iohexolum inn - stungulyf, lausn - 140 mg j/ml
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
prednisolon eql pharma tafla 5 mg
eql pharma ab - prednisolonum inn - tafla - 5 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
aburic filmuhúðuð tafla 80 mg
williams & halls ehf. - febuxostatum inn - filmuhúðuð tafla - 80 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
baklofen viatris (baklofen mylan) tafla 10 mg
viatris limited - baclofenum inn - tafla - 10 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
baklofen viatris (baklofen mylan) tafla 25 mg
viatris limited - baclofenum inn - tafla - 25 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
depo-medrol stungulyf, dreifa 40 mg/ml
pfizer aps - methylprednisolonum acetat - stungulyf, dreifa - 40 mg/ml