Asasantin Retard 200 mg / 25 mg Norge - norsk - Statens legemiddelverk

asasantin retard 200 mg / 25 mg

boehringer ingelheim international gmbh - dipyridamol / acetylsalisylsyre - kapsel med modifisert frisetting, hard - 200 mg / 25 mg

Creon 10000 Norge - norsk - Statens legemiddelverk

creon 10000

viatris as - lipase / amylase / protease - enterokapsel, hard - 10000 ie / 8000 ie / 600 ie

Creon 25000 Norge - norsk - Statens legemiddelverk

creon 25000

viatris as - lipase / amylase / protease - enterokapsel, hard - 25000 ie / 18000 ie / 1000 ie

Creon 40000 Norge - norsk - Statens legemiddelverk

creon 40000

mylan - asker - lipase / amylase / protease - enterokapsel, hard - 40000 e / 25000 e / 1600 e

Aponova 200 mg Norge - norsk - Statens legemiddelverk

aponova 200 mg

alternova - dipyridamol - depotkapsel, hard - 200 mg

Nurofen 100 mg Norge - norsk - Statens legemiddelverk

nurofen 100 mg

reckitt benckiser healthcare (nordics) a/s - ibuprofen - tyggekapsel, myk - 100 mg

Persantin Retard 200 mg Norge - norsk - Statens legemiddelverk

persantin retard 200 mg

boehringer ingelheim international gmbh - dipyridamol - kapsel med modifisert frisetting, hard - 200 mg

Toilax 5 mg Norge - norsk - Statens legemiddelverk

toilax 5 mg

orion corporation orion pharma - bisakodyl - enterotablett - 5 mg

Toilax Kombinasjonspakning 10 mg/ dose / 5 mg Norge - norsk - Statens legemiddelverk

toilax kombinasjonspakning 10 mg/ dose / 5 mg

orion corporation orion pharma, espoo - bisakodyl - enterotablett, rektalvæske, suspensjon - 10 mg/ dose / 5 mg

Symkevi Den europeiske union - norsk - EMA (European Medicines Agency)

symkevi

vertex pharmaceuticals (ireland) limited - tezacaftor, ivacaftor - cystisk fibrose - andre åndedrettsprodukter - symkevi is indicated in a combination regimen with ivacaftor tablets for the treatment of patients with cystic fibrosis (cf) aged 6 years and older who are homozygous for the f508del mutation or who are heterozygous for the f508del mutation and have one of the following mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene: p67l, r117c, l206w, r352q, a455e, d579g, 711+3a→g, s945l, s977f, r1070w, d1152h, 2789+5g→a, 3272 26a→g, and 3849+10kbc→t.