Animed vet (Anispray) Húðúði, dreifa 2,45 % w/w Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

animed vet (anispray) húðúði, dreifa 2,45 % w/w

animedica gmbh* - chlortetracycline hydrochloride - húðúði, dreifa - 2,45 % w/w

Vumerity Evrópusambandið - íslenska - EMA (European Medicines Agency)

vumerity

biogen netherlands b.v. - diroximel fumarate (biib098) - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).

Genestran Vet Stungulyf, lausn 75 míkróg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

genestran vet stungulyf, lausn 75 míkróg/ml

animedica gmbh* - cloprostenolum natríum - stungulyf, lausn - 75 míkróg/ml

Menbutil (Genabiline) Stungulyf, lausn 100 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

menbutil (genabiline) stungulyf, lausn 100 mg/ml

animedica gmbh - menbutone - stungulyf, lausn - 100 mg/ml

Enrotron Flavour (Enrotron) Tafla 150 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

enrotron flavour (enrotron) tafla 150 mg

animedica gmbh* - enrofloxacinum inn - tafla - 150 mg

Enrotron Flavour Tafla 50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

enrotron flavour tafla 50 mg

animedica gmbh* - enrofloxacinum inn - tafla - 50 mg

Morphasol vet Stungulyf, lausn 4 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

morphasol vet stungulyf, lausn 4 mg/ml

animedica gmbh* - butorphanolum tartrat - stungulyf, lausn - 4 mg/ml

Procapen vet Spenalyf, dreifa 3 g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

procapen vet spenalyf, dreifa 3 g

animedica gmbh* - benzylpenicillinprocainum - spenalyf, dreifa - 3 g

Torphasol vet (Morphasol) Stungulyf, lausn 10 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

torphasol vet (morphasol) stungulyf, lausn 10 mg/ml

animedica gmbh* - butorphanolum tartrat - stungulyf, lausn - 10 mg/ml

Prepandrix Evrópusambandið - íslenska - EMA (European Medicines Agency)

prepandrix

glaxosmithkline biologicals s.a. - a / indonesia / 05/2005 (h5n1) eins og álag notað (pr8-ibcdc-rg2) - influenza, human; immunization; disease outbreaks - bóluefni - virkt bólusetning gegn h5n1 undirflokk inflúensu-a vírus. Þetta merki er byggt á immunogenicity gögn úr heilbrigðum einstaklingar frá 18 ára aldri og áfram eftir gjöf tvo skammta af bóluefni tilbúinn með h5n1 undirgerð stofnar. prepandrix ætti að vera notuð í samræmi við opinbera leiðsögn.