Cordarone 200 mg Norvēģija - norvēģu - Statens legemiddelverk

cordarone 200 mg

sanofi-aventis norge (3) - amiodaronhydroklorid - tablett - 200 mg

Duodart 0.5 mg / 0.4 mg Norvēģija - norvēģu - Statens legemiddelverk

duodart 0.5 mg / 0.4 mg

glaxosmithkline as - dutasterid / tamsulosinhydroklorid - kapsel, hard - 0.5 mg / 0.4 mg

Ketamin Abcur 10 mg/ ml Norvēģija - norvēģu - Statens legemiddelverk

ketamin abcur 10 mg/ ml

abcur ab - ketaminhydroklorid - injeksjonsvæske, oppløsning - 10 mg/ ml

Ketamin Abcur 50 mg/ ml Norvēģija - norvēģu - Statens legemiddelverk

ketamin abcur 50 mg/ ml

abcur ab - ketaminhydroklorid - injeksjonsvæske, oppløsning - 50 mg/ ml

Rimstar Norvēģija - norvēģu - Statens legemiddelverk

rimstar

sandoz - københavn - rifampicin / isoniazid / pyrazinamid / etambutolhydroklorid - tablett, filmdrasjert - 150 mg / 75 mg / 400 mg / 275 mg

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

sixmo

l. molteni & c. dei fratelli alitti società di esercizio s.p.a. - buprenorfin hydrochloride - opioid-relaterte lidelser - andre nervesystemet narkotika - sixmo er indikert for substitusjonsbehandling for opioidavhengighet i klinisk stabil voksne pasienter som ikke krever mer enn 8 mg/dag sublingual buprenorfin, innenfor en ramme av medisinsk, sosial og psykologisk behandling.

Amiodaron Hameln 50 mg/ ml Norvēģija - norvēģu - Statens legemiddelverk

amiodaron hameln 50 mg/ ml

hameln pharma gmbh - amiodaronhydroklorid - konsentrat til injeksjons-/infusjonsvæske, oppløsning - 50 mg/ ml

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.

Dutasteride/Tamsulosin Hexal 0.5 mg / 0.4 mg Norvēģija - norvēģu - Statens legemiddelverk

dutasteride/tamsulosin hexal 0.5 mg / 0.4 mg

hexal a/s - dutasterid / tamsulosinhydroklorid - kapsel, hard - 0.5 mg / 0.4 mg

Dutasteride/Tamsulosin Orion 0.5 mg / 0.4 mg Norvēģija - norvēģu - Statens legemiddelverk

dutasteride/tamsulosin orion 0.5 mg / 0.4 mg

orion corporation - espoo - dutasterid / tamsulosinhydroklorid - kapsel, hard - 0.5 mg / 0.4 mg