Haldol 1 mg Noorwegen - Noors - Statens legemiddelverk

haldol 1 mg

essential pharma limited - haloperidol - tablett - 1 mg

Subutex 8 mg Noorwegen - Noors - Statens legemiddelverk

subutex 8 mg

indivior europe limited - buprenorfinhydroklorid - sublingvaltablett - 8 mg

Subutex 2 mg Noorwegen - Noors - Statens legemiddelverk

subutex 2 mg

indivior europe limited - buprenorfinhydroklorid - sublingvaltablett - 2 mg

Terbinafin Bluefish 250 mg Noorwegen - Noors - Statens legemiddelverk

terbinafin bluefish 250 mg

bluefish pharmaceuticals ab - terbinafinhydroklorid - tablett - 250 mg

Hulio Europese Unie - Noors - EMA (European Medicines Agency)

hulio

biosimilar collaborations ireland limited - adalimumab - hidradenitis suppurativa; psoriasis; uveitis; arthritis, rheumatoid; spondylitis, ankylosing; crohn disease; colitis, ulcerative; arthritis, psoriatic - immunosuppressants, tumor nekrose faktor alfa (tnf-α) - hemmere

Inbrija Europese Unie - Noors - EMA (European Medicines Agency)

inbrija

acorda therapeutics ireland limited - levodopa - parkinsonsykdom - anti-parkinson medisiner - inbrija er indikert for intermitterende behandling av episodisk motoriske fluktuasjoner (av episoder) hos voksne pasienter med parkinsons sykdom (pd) behandlet med levodopa/dopa-decarboxylase inhibitor.

Kaftrio Europese Unie - Noors - EMA (European Medicines Agency)

kaftrio

vertex pharmaceuticals (ireland) limited - ivacaftor, tezacaftor, elexacaftor - cystisk fibrose - andre åndedrettsprodukter - kaftrio is indicated in a combination regimen with ivacaftor for the treatment of cystic fibrosis (cf) in patients aged 6 years and older who have at least one f508del mutation in the cystic fibrosis transmembrane conductance regulator (cftr) gene.

Celsunax Europese Unie - Noors - EMA (European Medicines Agency)

celsunax

pinax pharma gmbh - ioflupane (123i) - radionuclide imaging; dementia; movement disorders - diagnostiske radiopharmaceuticals - dette legemidlet er kun til diagnostisk bruk. celsunax is indicated for detecting loss of functional dopaminergic neuron terminals in the striatum:in adult patients with clinically uncertain parkinsonian syndromes, for example those with early symptoms, in order to help differentiate essential tremor from parkinsonian syndromes related to idiopathic parkinson’s disease, multiple system atrophy and progressive supranuclear palsy.  celsunax is unable to discriminate between parkinson's disease, multiple system atrophy and progressive supranuclear palsy. hos voksne pasienter, for å kunne skille mellom sannsynlig demens med lewy legemer fra alzheimers sykdom.  celsunax is unable to discriminate between dementia with lewy bodies and parkinson’s disease dementia.

Xevudy Europese Unie - Noors - EMA (European Medicines Agency)

xevudy

glaxosmithkline trading services limited - sotrovimab - covid-19 virus infection - immune sera og immunglobuliner, - xevudy is indicated for the treatment of adults and adolescents (aged 12 years and over and weighing at least 40 kg) with coronavirus disease 2019 (covid-19) who do not require oxygen supplementation and who are at increased risk of progressing to severe covid-19.

Lextemy Europese Unie - Noors - EMA (European Medicines Agency)

lextemy

mylan ire healthcare limited - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastiske midler - treatment of carcinoma of the colon or rectum, breast cancer, non-small cell lung cancer, renal cell cancer, epithelial ovarian, fallopian tube or primary peritoneal cancer, and carcinoma of the cervix.