Besremi Europos Sąjunga - islandų - EMA (European Medicines Agency)

besremi

aop orphan pharmaceuticals gmbh - ropeginterferon alfa-2b - blóðríki - Ónæmisörvandi, - besremi er ætlað eitt og sér í fullorðnir fyrir meðferð polycythaemia vera án einkenna miltisstækkun.

Opdualag Europos Sąjunga - islandų - EMA (European Medicines Agency)

opdualag

bristol-myers squibb pharma eeig - nivolumab, relatlimab - melanoma - antineoplastic agents, monoclonal antibodies - opdualag is indicated for the first line treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older with tumour cell pd l1 expression < 1%.

Bupropion Teva Tafla með breyttan losunarhraða 300 mg Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

bupropion teva tafla með breyttan losunarhraða 300 mg

teva b.v.* - bupropionum hýdróklóríð - tafla með breyttan losunarhraða - 300 mg

Bupropion Teva Tafla með breyttan losunarhraða 150 mg Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

bupropion teva tafla með breyttan losunarhraða 150 mg

teva b.v.* - bupropionum hýdróklóríð - tafla með breyttan losunarhraða - 150 mg

Propolipid Stungulyf/innrennslislyf, fleyti 10 mg/ml Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

propolipid stungulyf/innrennslislyf, fleyti 10 mg/ml

fresenius kabi ab - propofolum inn - stungulyf/innrennslislyf, fleyti - 10 mg/ml

Zitromax Filmuhúðuð tafla 500 mg Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

zitromax filmuhúðuð tafla 500 mg

pfizer aps - azithromycinum díhýdrat - filmuhúðuð tafla - 500 mg

Zitromax Mixtúruduft, dreifa 40 mg/ml Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

zitromax mixtúruduft, dreifa 40 mg/ml

pfizer aps - azithromycinum díhýdrat - mixtúruduft, dreifa - 40 mg/ml

Lamictal Tuggu-/dreifitafla 50 mg Islandija - islandų - LYFJASTOFNUN (Icelandic Medicines Agency)

lamictal tuggu-/dreifitafla 50 mg

glaxosmithkline pharma a/s - lamotriginum inn - tuggu-/dreifitafla - 50 mg