Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

virbac s.a. - levende dempet rabiesvirus, sag2-stamme - live viral vaksiner - raccoon dogs (nyctereutes procyonoides); red foxes (vulpes vulpes) - for aktiv immunisering av røde ræv og vaskehunder for å forhindre infeksjon med rabiesvirus. varigheten av beskyttelsen er på minst 6 måneder.

Նորվեգիա - Նորվեգերեն - Statens legemiddelverk

intervet international bv - 5831 an - isofluran - væske til inhalasjonsdamp - 100 % w/w

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vaksiner - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. bruk av denne vaksinen skal være i samsvar med offisielle anbefalinger.

Նորվեգիա - Նորվեգերեն - Statens legemiddelverk

vetpharma as - benzylpenicillinprokain - intramammarie, salve - 300 mg

Նորվեգիա - Նորվեգերեն - Statens legemiddelverk

boehringer ingelheim animal health nordics - benzylpenicillinprokain / dihydrostreptomycinsulfat - intramammarie, salve - 500 mg / 1 g

Նորվեգիա - Նորվեգերեն - Statens legemiddelverk

boehringer ingelheim animal health nordics - benzylpenicillinprokain / dihydrostreptomycinsulfat - intramammarie, salve - 200 mg / 200 mg

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

dendreon uk ltd - autologous perifere blod mononukleære celler inkludert minst 50 millioner autologous cd54 + celler aktivert med prostatic sure fosfatase granulocytt-macrophage koloni-stimulerende faktor - prostata neoplasmer - andre immunstimulerende midler - provenge er indisert for behandling av asymptomatisk eller minimalt symptomatisk metastatisk (ikke-visceral) castratresistent prostatakreft hos mannlige voksne der kjemoterapi ennå ikke er klinisk indikert.

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

intervet international bv - halofuginone - antiprotozoals - kalver, nyfødte - i nyfødt calvesprevention av diaré på grunn av diagnostisert cryptosporidium parvum i gårder med historie cryptosporidiosis. administrasjonen skal starte i de første 24 til 48 timer. reduksjon av diaré på grunn av diagnostisert cryptosporidium parvum. administrasjon skal starte innen 24 timer etter at diaréen har begynt. i begge tilfeller, reduksjon av oocyst utskillelse har blitt vist.

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

dompe farmaceutici s.p.a. - recombinant human nerve growth factor - keratitt - Øyemidler - behandling av moderat (vedvarende epitelfeil) eller alvorlig (hornhinnenssår) nevrotrofisk keratitt hos voksne.

Նորվեգիա - Նորվեգերեն - Statens legemiddelverk

alternova - baklofen - injeksjons-/infusjonsvæske, oppløsning - 0.5 mg/ ml