Benferol 25000 IU Norvēģija - norvēģu - Statens legemiddelverk

benferol 25000 iu

consilient health limited - kolekalsiferol - kapsel, myk - 25000 iu

Benferol 50000 IU Norvēģija - norvēģu - Statens legemiddelverk

benferol 50000 iu

consilient health limited - kolekalsiferol - kapsel, myk - 50000 iu

Kenacort-T 40 mg/ ml Norvēģija - norvēģu - Statens legemiddelverk

kenacort-t 40 mg/ ml

bristol-myers squibb ab - triamcinolonacetonid - injeksjonsvæske, suspensjon - 40 mg/ ml

Mezavant 1200 mg Norvēģija - norvēģu - Statens legemiddelverk

mezavant 1200 mg

takeda pharmaceuticals international ag ireland branch - mesalazin - enterodepottablett - 1200 mg

Mivacron 2 mg/ ml Norvēģija - norvēģu - Statens legemiddelverk

mivacron 2 mg/ ml

aspen pharma trading limited - mivakuriumklorid - injeksjonsvæske, oppløsning - 2 mg/ ml

Ultiva 2 mg Norvēģija - norvēģu - Statens legemiddelverk

ultiva 2 mg

aspen pharma trading limited - remifentanilhydroklorid - pulver til injeksjons-/infusjonsvæske, oppløsning - 2 mg

Ultiva 1 mg Norvēģija - norvēģu - Statens legemiddelverk

ultiva 1 mg

aspen pharma trading limited - remifentanilhydroklorid - pulver til injeksjons-/infusjonsvæske, oppløsning - 1 mg

Ultiva 5 mg Norvēģija - norvēģu - Statens legemiddelverk

ultiva 5 mg

aspen pharma trading limited - remifentanilhydroklorid - pulver til injeksjons-/infusjonsvæske, oppløsning - 5 mg

Bencium 500 mg / 800 IU Norvēģija - norvēģu - Statens legemiddelverk

bencium 500 mg / 800 iu

consilient health limited - kalsiumkarbonat / kolekalsiferol - tyggetablett med appelsinsmak - 500 mg / 800 iu

Zeposia Eiropas Savienība - norvēģu - EMA (European Medicines Agency)

zeposia

bristol-myers squibb pharma eeig - ozanimod hydrochloride - multiple sclerosis, relapsing-remitting; colitis, ulcerative - immunsuppressive - multiple sclerosiszeposia is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (rrms) with active disease as defined by clinical or imaging features. ulcerative colitiszeposia is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent.