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

zeleris

ceva santé animale - florfenicol, meloxicam - amphenicols, sturtu, sýklalyf fyrir almenn nota - nautgripir - til lækninga meðferð nautgripum sjúkdóma í öndunarfærum (brd) í tengslum við hiti vegna mannheimia haemolytica, pasteurella multocida og histophilus somni næm florfenicol.

Hirudoid Krem 3 mg/g Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

hirudoid krem 3 mg/g

stada arzneimittel ag - heparinoidum ex organis animal - krem - 3 mg/g

Hirudoid Hlaup 3 mg/g Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

hirudoid hlaup 3 mg/g

stada arzneimittel ag - heparinoidum ex organis animal - hlaup - 3 mg/g

Lomudal Augndropar, lausn 20 mg/ml Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

lomudal augndropar, lausn 20 mg/ml

stada arzneimittel ag - sodium cromoglicate - augndropar, lausn - 20 mg/ml

Malastad Filmuhúðuð tafla 250/100mg mg Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

malastad filmuhúðuð tafla 250/100mg mg

stada arzneimittel ag - atovaquonum inn; proguanilum hýdróklóríð - filmuhúðuð tafla - 250/100mg mg

Marbodin Filmuhúðuð tafla 10 mg Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

marbodin filmuhúðuð tafla 10 mg

stada arzneimittel ag - memantinum hýdróklóríð - filmuhúðuð tafla - 10 mg

Marbodin Filmuhúðuð tafla 20 mg Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

marbodin filmuhúðuð tafla 20 mg

stada arzneimittel ag - memantinum hýdróklóríð - filmuhúðuð tafla - 20 mg

Tavegyl Tafla 1 mg Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

tavegyl tafla 1 mg

stada arzneimittel ag - clemastinum fúmarat - tafla - 1 mg

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

kinpeygo

stada arzneimittel ag - budesonide, micronised - glomerulonephritis, iga - antidiarrheals, þarma bólgueyðandi / antiinfective lyfjum - kinpeygo is indicated for the treatment of primary immunoglobulin a (iga) nephropathy (igan) in adults at risk of rapid disease progression with a urine protein-to-creatinine ratio (upcr) ≥1. 5 g/gram.

Amiloride/HCT Alvogen (Diuramin) Tafla 5/50 mg Islanda - Iżlandiż - LYFJASTOFNUN (Icelandic Medicines Agency)

amiloride/hct alvogen (diuramin) tafla 5/50 mg

alvogen ehf. - amiloridum hýdróklóríð; hydrochlorothiazidum inn - tafla - 5/50 mg