Diprospan Stungulyf, dreifa 5+2 mg/ml Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

diprospan stungulyf, dreifa 5+2 mg/ml

n.v. organon* - betamethasonum dínatríumfosfat; betamethasonum díprópíónat - stungulyf, dreifa - 5+2 mg/ml

Kenacort-T Stungulyf, dreifa 40 mg/ml Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

kenacort-t stungulyf, dreifa 40 mg/ml

bristol-myers squibb ab - triamcinolonum acetóníð - stungulyf, dreifa - 40 mg/ml

Zofran Mixtúra, lausn 0,8 mg/ml Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

zofran mixtúra, lausn 0,8 mg/ml

sandoz a/s - ondansetronum hýdróklóríð - mixtúra, lausn - 0,8 mg/ml

Zovirax (Zovir) Mixtúra, dreifa 80 mg/ml Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

zovirax (zovir) mixtúra, dreifa 80 mg/ml

glaxosmithkline pharma a/s - aciclovirum inn - mixtúra, dreifa - 80 mg/ml

Amoxicillin Sandoz Mixtúruduft, dreifa 100 mg/ml Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

amoxicillin sandoz mixtúruduft, dreifa 100 mg/ml

sandoz a/s* - amoxicillinum tríhýdrat - mixtúruduft, dreifa - 100 mg/ml

Azithromycin STADA Mixtúruduft, dreifa 40 mg/ml Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

azithromycin stada mixtúruduft, dreifa 40 mg/ml

stada arzneimittel ag - azithromycinum díhýdrat - mixtúruduft, dreifa - 40 mg/ml

Diclofenac Teva Hlaup 23,2 mg/g Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

diclofenac teva hlaup 23,2 mg/g

teva b.v.* - diclofenacum tvíetýlamín - hlaup - 23,2 mg/g

Fulvestrant Teva Stungulyf, lausn í áfylltri sprautu 250 mg Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

fulvestrant teva stungulyf, lausn í áfylltri sprautu 250 mg

teva b.v.* - fulvestrantum inn - stungulyf, lausn í áfylltri sprautu - 250 mg

Aerius Unjoni Ewropea - Iżlandiż - EMA (European Medicines Agency)

aerius

n.v. organon - desloratadin - rhinitis, allergic, perennial; urticaria; rhinitis, allergic, seasonal - andhistamín fyrir almenn nota, - aerius er ætlað til að draga af einkennum:ofnæmi nefi;ofsakláða.

Azomyr Unjoni Ewropea - Iżlandiż - EMA (European Medicines Agency)

azomyr

n.v. organon - desloratadin - rhinitis, allergic, perennial; urticaria; rhinitis, allergic, seasonal - andhistamín fyrir almenn nota, - azomyr is indicated for the relief of symptoms associated with:allergic rhinitis (see section 5. 1)urticaria (see section 5.