Ucedane Evrópusambandið - íslenska - EMA (European Medicines Agency)

ucedane

eurocept international bv - carglumic acid - hyperammonemia; amino acid metabolism, inborn errors - Önnur meltingarvegi og efnaskipti vörur, - ucedane is indicated in treatment of:hyperammonaemia due to n-acetylglutamate synthase primary deficiency;hyperammonaemia due to isovaleric acidaemia;hyperammonaemia due to methymalonic acidaemia;hyperammonaemia due to propionic acidaemia.

Gaviscon Mixtúra, dreifa Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

gaviscon mixtúra, dreifa

nordic drugs ab - calcii carbonas; aluminii hydroxidum; natrii hydrogenocarbonas; natrii alginas - mixtúra, dreifa

Gaviscon Tuggutafla Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

gaviscon tuggutafla

nordic drugs ab - aluminium hydroxide; sodium hydrogen carbonate; acidum alginicum - tuggutafla

Xenpozyme Evrópusambandið - íslenska - EMA (European Medicines Agency)

xenpozyme

sanofi b.v. - olipudase alfa - acid sphingomyelinase deficiency (asmd) type a/b or type b - Önnur meltingarvegi og efnaskipti vörur, - xenpozyme is indicated as an enzyme replacement therapy for the treatment of non-central nervous system (cns) manifestations of acid sphingomyelinase deficiency (asmd) in paediatric and adult patients with type a/b or type b.

Fucidin-Hydrocortison Krem 20 + 10 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

fucidin-hydrocortison krem 20 + 10 mg

leo pharma a/s* - acidum fusidicum inn; hydrocortisonum acetat - krem - 20 + 10 mg

Niontix Lyfjagas, fljótandi 100% Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

niontix lyfjagas, fljótandi 100%

linde sverige ab - dinitrogenii oxidum - lyfjagas, fljótandi - 100%

Spectracillin Filmuhúðuð tafla 875/125 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

spectracillin filmuhúðuð tafla 875/125 mg

williams & halls ehf. - acidum clavulanicum kalíum; amoxicillinum tríhýdrat - filmuhúðuð tafla - 875/125 mg

Segluromet Evrópusambandið - íslenska - EMA (European Medicines Agency)

segluromet

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - sykursýki, tegund 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.