Finilac Mixtúra, lausn 50 míkróg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

finilac mixtúra, lausn 50 míkróg/ml

le vet beheer b.v. - cabergolinum inn - mixtúra, lausn - 50 míkróg/ml

Benestermycin vet. Spenalyf, smyrsli Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

benestermycin vet. spenalyf, smyrsli

boehringer ingelheim vetmedica gmbh* - framycetinum súlfat; benethaminum penicillinum inn; penethamate hydroiodide ban - spenalyf, smyrsli

Procamidor vet. Stungulyf, lausn 20 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

procamidor vet. stungulyf, lausn 20 mg/ml

vetviva richter gmbh - procainum hýdróklóríð - stungulyf, lausn - 20 mg/ml

Paxetin Filmuhúðuð tafla 20 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

paxetin filmuhúðuð tafla 20 mg

teva b.v.* - paroxetinum hýdróklóríð - filmuhúðuð tafla - 20 mg

Seroxat Filmuhúðuð tafla 20 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

seroxat filmuhúðuð tafla 20 mg

glaxosmithkline pharma a/s - paroxetinum hýdróklóríð - filmuhúðuð tafla - 20 mg

Seroxat Filmuhúðuð tafla 10 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

seroxat filmuhúðuð tafla 10 mg

glaxosmithkline pharma a/s - paroxetinum hýdróklóríð - filmuhúðuð tafla - 10 mg

Sumatriptan Bluefish Tafla 100 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sumatriptan bluefish tafla 100 mg

bluefish pharmaceuticals ab - sumatriptanum súkkínat - tafla - 100 mg

Sumatriptan Bluefish Tafla 50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sumatriptan bluefish tafla 50 mg

bluefish pharmaceuticals ab - sumatriptanum súkkínat - tafla - 50 mg

Trimbow Evrópusambandið - íslenska - EMA (European Medicines Agency)

trimbow

chiesi farmaceutici s.p.a. - beclometasone dipropionate, formóteróli fúmarat tvíhýdrat, Þannig brómíð - lungnasjúkdómur, langvarandi hindrandi - lyf til veikindi öndunarvegi sjúkdómum, - maintenance treatment of asthma, in adults not adequately controlled with a maintenance combination of a long-acting beta2-agonist and high dose of inhaled corticosteroid, and who experienced one or more asthma exacerbations in the previous year. copdmaintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (copd) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2-agonist or a combination of a long-acting beta2-agonist and a long-acting muscarinic antagonist (for effects on symptoms control and prevention of exacerbations see section 5. asthmamaintenance treatment of asthma, in adults not adequately controlled with a maintenance combination of a long-acting beta2-agonist and medium dose of inhaled corticosteroid, and who experienced one or more asthma exacerbations in the previous year.

Riarify (previously CHF 5993 Chiesi Farmaceutici S.p.A.) Evrópusambandið - íslenska - EMA (European Medicines Agency)

riarify (previously chf 5993 chiesi farmaceutici s.p.a.)

chiesi farmaceutici s.p.a. - formoterol fumarate dihydrate, glycopyrronium, beclometasone dipropionate - lungnasjúkdómur, langvarandi hindrandi - lyf til veikindi öndunarvegi sjúkdómum, - viðhald meðferð í fullorðinn sjúklinga með í meðallagi til alvarlega langvinn veikindi í lungum (llt) sem eru ekki nægilega meðhöndluð með sambland af andað barksteri og langverkandi beta-2-örva (fyrir áhrif á einkenni stjórn og koma í veg fyrir tilvikum sjá kafla 5.