Seffalair Spiromax European Union - Icelandic - EMA (European Medicines Agency)

seffalair spiromax

teva b.v. - fluticasone propionate, salmeterol xinafoate - astma - lyf til veikindi öndunarvegi sjúkdómum, - seffalair spiromax is indicated in the regular treatment of asthma in adults and adolescents aged 12 years and older not adequately controlled with inhaled corticosteroids and ‘as needed’ inhaled short-acting β₂ agonists.

Flutiform (Affilia) Innúðalyf, dreifa 125 míkróg/5 míkróg Iceland - Icelandic - LYFJASTOFNUN (Icelandic Medicines Agency)

flutiform (affilia) innúðalyf, dreifa 125 míkróg/5 míkróg

mundipharma a/s - fluticasonum própíónat; formoterolum fúmarat - innúðalyf, dreifa - 125 míkróg/5 míkróg

Flutiform (Affilia) Innúðalyf, dreifa 250 míkróg/10 míkróg Iceland - Icelandic - LYFJASTOFNUN (Icelandic Medicines Agency)

flutiform (affilia) innúðalyf, dreifa 250 míkróg/10 míkróg

mundipharma a/s - fluticasonum própíónat; formoterolum fúmarat - innúðalyf, dreifa - 250 míkróg/10 míkróg

Flutiform (Affilia) Innúðalyf, dreifa 50 míkróg/5 míkróg Iceland - Icelandic - LYFJASTOFNUN (Icelandic Medicines Agency)

flutiform (affilia) innúðalyf, dreifa 50 míkróg/5 míkróg

mundipharma a/s - fluticasonum própíónat; formoterolum fúmarat - innúðalyf, dreifa - 50 míkróg/5 míkróg

Seretide Innöndunarduft, afmældir skammtar 50/250 míkróg/skammt Iceland - Icelandic - LYFJASTOFNUN (Icelandic Medicines Agency)

seretide innöndunarduft, afmældir skammtar 50/250 míkróg/skammt

glaxosmithkline pharma a/s - fluticasonum própíónat; salmeterolum xínafóat - innöndunarduft, afmældir skammtar - 50/250 míkróg/skammt

Seretide Innöndunarduft, afmældir skammtar 50/500 míkróg/skammt Iceland - Icelandic - LYFJASTOFNUN (Icelandic Medicines Agency)

seretide innöndunarduft, afmældir skammtar 50/500 míkróg/skammt

glaxosmithkline pharma a/s - fluticasonum própíónat; salmeterolum xínafóat - innöndunarduft, afmældir skammtar - 50/500 míkróg/skammt

Dymista Nefúði, dreifa 137 míkróg / 50 míkróg/skammt Iceland - Icelandic - LYFJASTOFNUN (Icelandic Medicines Agency)

dymista nefúði, dreifa 137 míkróg / 50 míkróg/skammt

viatris aps - azelastinum hýdróklóríð; fluticasonum própíónat - nefúði, dreifa - 137 míkróg / 50 míkróg/skammt

Atectura Breezhaler European Union - Icelandic - EMA (European Medicines Agency)

atectura breezhaler

novartis europharm limited  - indacaterol acetate, mometasone furoate - astma - lyf til veikindi öndunarvegi sjúkdómum, - atectura breezhaler is indicated as a maintenance treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Bemrist Breezhaler European Union - Icelandic - EMA (European Medicines Agency)

bemrist breezhaler

novartis europharm limited  - indacaterol, mometasone furoate - astma - lyf til veikindi öndunarvegi sjúkdómum, - bemrist breezhaler is indicated as a maintenance   treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Enerzair Breezhaler European Union - Icelandic - EMA (European Medicines Agency)

enerzair breezhaler

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - astma - lyf til veikindi öndunarvegi sjúkdómum, - enerzair breezhaler is indicated as a maintenance treatment of asthma in adult patients not adequately controlled with a maintenance combination of a long acting beta2 agonist and a high dose of an inhaled corticosteroid who experienced one or more asthma exacerbations in the previous year.