Dolovet vet Duft til inntöku 160 mg/ g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

dolovet vet duft til inntöku 160 mg/ g

vetcare oy - ketoprofenum inn - duft til inntöku - 160 mg/ g

Ketodine vet. (Ketodolor) Stungulyf, lausn 100 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

ketodine vet. (ketodolor) stungulyf, lausn 100 mg/ml

le vet beheer b.v. - ketoprofenum inn - stungulyf, lausn - 100 mg/ml

Romefen vet. Stungulyf, lausn 100 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

romefen vet. stungulyf, lausn 100 mg/ml

ceva santé animale* - ketoprofenum inn - stungulyf, lausn - 100 mg/ml

Orudis Hart forðahylki 100 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

orudis hart forðahylki 100 mg

sanofi-aventis norge as - ketoprofenum inn - hart forðahylki - 100 mg

Cholib Evrópusambandið - íslenska - EMA (European Medicines Agency)

cholib

viatris healthcare limited - fenófíbrat, simvastatin - dýrarannsóknir - lipid breytandi lyf - cholib er fram eins og venjulega meðferð til að fæði og æfing í mikilli hættu hjarta fullorðinn sjúklinga með blönduðum dyslipidaemia til að draga úr kalíum og auka gegn c stigum þegar gegn c stigum eru nægilega stjórnað með sama skammt af sér simvastatin.

Zaditen Augndropar, lausn í stakskammtaíláti 0,25 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

zaditen augndropar, lausn í stakskammtaíláti 0,25 mg/ml

laboratoires thea s.a.s. - ketotifenum fúmarat - augndropar, lausn í stakskammtaíláti - 0,25 mg/ml

Zaditen Augndropar, lausn 0,25 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

zaditen augndropar, lausn 0,25 mg/ml

laboratoires thea s.a.s. - ketotifenum fúmarat - augndropar, lausn - 0,25 mg/ml

Aubagio Evrópusambandið - íslenska - EMA (European Medicines Agency)

aubagio

sanofi winthrop industrie - teriflunomide - margvísleg sclerosis - valdar ónæmisbælandi lyf - aubagio is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Teriflunomide Mylan Evrópusambandið - íslenska - EMA (European Medicines Agency)

teriflunomide mylan

mylan pharmaceuticals limited - teriflunomide - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi lyf - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Teriflunomide Accord Evrópusambandið - íslenska - EMA (European Medicines Agency)

teriflunomide accord

accord healthcare s.l.u. - teriflunomide - heila-og mænusigg, köstum tilkynnt - Ónæmisbælandi, sérhæfður ónæmisbælandi - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).