Abstral Tungurótartafla 300 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 300 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 300 míkróg

Abstral Tungurótartafla 200 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 200 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 200 míkróg

Abstral Tungurótartafla 100 míkróg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

abstral tungurótartafla 100 míkróg

kyowa kirin holdings b.v. - fentanylum cítrat - tungurótartafla - 100 míkróg

Norgesic 35 mg/450 mg Tafla 35+450 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

norgesic 35 mg/450 mg tafla 35+450 mg

viatris aps - orphenadrinum cítrat; paracetamolum inn - tafla - 35+450 mg

Duloxetine Lilly Evrópusambandið - íslenska - EMA (European Medicines Agency)

duloxetine lilly

eli lilly nederland b.v. - duloxetin - neuralgia; diabetic neuropathies; depressive disorder, major - psychoanaleptics, - duloxetine lilly er fram í fyrir fullorðna:meðferð helstu þunglyndi disordertreatment sykursýki útlæga taugakvillaverkur paintreatment af almenn kvíða disorderduloxetine lilly er ætlað í fullorðnir.

Malaseb vet. Hársápa 2 % w/v Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

malaseb vet. hársápa 2 % w/v

dechra veterinary products a/s* - chlorhexidinum díglúkónat; miconazolum nítrat - hársápa - 2 % w/v

Daktacort Krem Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

daktacort krem

mcneil sweden ab - miconazolum nítrat; hydrocortisonum inn - krem

Tamoxifen Mylan Tafla 20 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

tamoxifen mylan tafla 20 mg

viatris limited - tamoxifenum cítrat - tafla - 20 mg

Saniotic vet. (Mitex vet.) Eyrnadropar/húðdreifa 5,0 mg/0,5293 mg/23,0 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

saniotic vet. (mitex vet.) eyrnadropar/húðdreifa 5,0 mg/0,5293 mg/23,0 mg/ml

vetviva richter gmbh - miconazolum nítrat; prednisolonum acetat; polymyxinum b súlfat - eyrnadropar/húðdreifa - 5,0 mg/0,5293 mg/23,0 mg/ml

Prepandemic influenza vaccine (H5N1) (surface antigen, inactivated, adjuvanted) Novartis Vaccines and Diagnostics Evrópusambandið - íslenska - EMA (European Medicines Agency)

prepandemic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted) novartis vaccines and diagnostics

novartis vaccines and diagnostics s.r.l. - yfirborðs mótefna gegn inflúensuveiru (haemagglutinin og neuraminidasa) á stofn a / viet nam / 1194/2004 (h5n1) - influenza, human; immunization; disease outbreaks - bóluefni - virkt bólusetning gegn h5n1 undirgerð inflúensu a veiru. , , this indication is based on immunogenicity data from healthy subjects from the age of 18 years onwards following administration of two doses of the vaccine containing a/vietnam/1194/2004 (h5n1)-like strain. , , prepandemic influenza vaccine (h5n1) novartis vaccines and diagnostic should be used in accordance with official recommendations.