Den Europæiske Union - islandsk - EMA (European Medicines Agency)

bayer animal health gmbh - iron(iii) ion, toltrazuril - toltrazuril, sturtu - svín (smágrísir) - fyrir samhliða fyrirbyggja klínískum merki um hníslasótt (eins og niðurgangur) í nýbura grísi á býli með staðfest sögu hníslasótt af völdum cystoisospora am, og koma í veg fyrir járn skort blóðleysi.

Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

stada arzneimittel ag - carvedilolum inn - tafla - 3,125 mg

Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

stada arzneimittel ag - carvedilolum inn - tafla - 6,25 mg

Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

stada arzneimittel ag - carvedilolum inn - tafla - 12,5 mg

Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

stada arzneimittel ag - carvedilolum inn - tafla - 25 mg

Den Europæiske Union - islandsk - EMA (European Medicines Agency)

ceva santé animale - benazepril hydrochloride, spironolactone - ÆÐakerfi - hundar - til meðferðar á hjartabilun vegna langvinna hrörnunarsjúkdóma í hundum (með þvagræsilyfjum eftir því sem við á).

Den Europæiske Union - islandsk - EMA (European Medicines Agency)

beigene ireland ltd - zanubrutinib - waldenstrom macroglobulinemia - Æxlishemjandi lyf - brukinsa as monotherapy is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. brukinsa as monotherapy is indicated for the treatment of adult patients with marginal zone lymphoma (mzl) who have received at least one prior anti-cd20-based therapy. brukinsa as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukemia (cll).

Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

pharmaq as - tricaine methane sulfonate - baðduft til meðhöndlunar fiska, lausn - 1000 mg/g

Island - islandsk - LYFJASTOFNUN (Icelandic Medicines Agency)

medical valley invest ab - ivermectinum inn - tafla - 3 mg

Den Europæiske Union - islandsk - EMA (European Medicines Agency)

zoetis belgium sa - toceranib - Æxlishemjandi lyf - hundar - meðferð við lifrarfrumukrabbamein í hundum sem ekki eru tilbúnir til endurtekninga (ii).