hirudoid hlaup 3 mg/g
stada arzneimittel ag - heparinoidum ex organis animal - hlaup - 3 mg/g
finasterid stada filmuhúðuð tafla 5 mg
stada arzneimittel ag - finasteridum inn - filmuhúðuð tafla - 5 mg
sevelamercarbonat stada filmuhúðuð tafla 800 mg
stada arzneimittel ag - sevelamerum karbónat - filmuhúðuð tafla - 800 mg
meropenem sun stungulyfs-/innrennslisstofn, lausn 1 g
sun pharmaceutical industries europe b.v. - meropenemum tríhýdrat - stungulyfs-/innrennslisstofn, lausn - 1 g
malastad filmuhúðuð tafla 250/100mg mg
stada arzneimittel ag - atovaquonum inn; proguanilum hýdróklóríð - filmuhúðuð tafla - 250/100mg mg
cetirizin stada filmuhúðuð tafla 10 mg
stada arzneimittel ag - cetirizinum díhýdróklóríð - filmuhúðuð tafla - 10 mg
finasterid stada filmuhúðuð tafla 1 mg
stada arzneimittel ag - finasteridum inn - filmuhúðuð tafla - 1 mg
meropenem sun stungulyfs-/innrennslisstofn, lausn 500 mg
sun pharmaceutical industries europe b.v. - meropenemum tríhýdrat - stungulyfs-/innrennslisstofn, lausn - 500 mg
arexvy
glaxosmithkline biologicals s.a. - respiratory syncytial virus recombinant glycoprotein f stabilised in the pre-fusion conformation (rsvpref3) produced in chinese hamster ovary (cho) cells by recombinant dna technology - sýkingar af völdum sýklalyfja - bóluefni - arexvy is indicated for active immunisation for the prevention of lower respiratory tract disease (lrtd) caused by respiratory syncytial virus in adults 60 years of age and older. notkun þetta bóluefni ætti að vera í samræmi við opinbera tillögur.
lomudal augndropar, lausn 20 mg/ml
stada arzneimittel ag - sodium cromoglicate - augndropar, lausn - 20 mg/ml