Ranitidin ratiopharm 75 mg Norge - norsk - Statens legemiddelverk

ranitidin ratiopharm 75 mg

ratiopharm gmbh - ranitidinhydroklorid - tablett, filmdrasjert - 75 mg

Ranitidin ratiopharm 150 mg Norge - norsk - Statens legemiddelverk

ranitidin ratiopharm 150 mg

ratiopharm gmbh - ranitidinhydroklorid - tablett, filmdrasjert - 150 mg

Ranitidin ratiopharm 300 mg Norge - norsk - Statens legemiddelverk

ranitidin ratiopharm 300 mg

ratiopharm gmbh - ranitidinhydroklorid - tablett, filmdrasjert - 300 mg

Zantac 25 mg/ ml Norge - norsk - Statens legemiddelverk

zantac 25 mg/ ml

glaxosmithkline as - ranitidinhydroklorid - injeksjonsvæske, oppløsning - 25 mg/ ml

Zantac 150 mg Norge - norsk - Statens legemiddelverk

zantac 150 mg

glaxosmithkline as - ranitidinhydroklorid - brusetablett - 150 mg

Zantac 150 mg Norge - norsk - Statens legemiddelverk

zantac 150 mg

glaxosmithkline as - ranitidinhydroklorid - tablett - 150 mg

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

ximluci

stada arzneimittel ag - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - Øyemidler - ximluci is indicated in adults for:the treatment of neovascular (wet) age-related macular degeneration (amd)the treatment of visual impairment due to diabetic macular oedema (dme)the treatment of proliferative diabetic retinopathy (pdr)the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)the treatment of visual impairment due to choroidal neovascularisation (cnv).

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

lucentis

novartis europharm limited - ranibizumab - wet macular degeneration; macular edema; diabetes complications; myopia, degenerative; choroidal neovascularization - Øyemidler - lucentis er angitt i voksne for:behandling av neovascular (våt) aldersrelatert makuladegenerasjon (amd)behandling av synshemming på grunn av choroidal neovascularisation (cnv)behandling av synshemming på grunn diabetiker macular ødemer (dme)behandling av synshemming på grunn av flekker ødemer sekundært til retinal vene okklusjon (gren rvo eller sentrale rvo).

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

byooviz

samsung bioepis nl b.v. - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; myopia, degenerative - Øyemidler - byooviz is indicated in adults for:the treatment of neovascular (wet) age-related macular degeneration (amd)the treatment of visual impairment due to diabetic macular oedema (dme)the treatment of proliferative diabetic retinopathy (pdr)the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)the treatment of visual impairment due to choroidal neovascularisation (cnv).

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

ranivisio

midas pharma gmbh - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - Øyemidler - ranivisio is indicated in adults for:• the treatment of neovascular (wet) age-related macular degeneration (amd)• the treatment of visual impairment due to diabetic macular oedema (dme)• the treatment of proliferative diabetic retinopathy (pdr)• the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)• the treatment of visual impairment due to choroidal neovascularisation (cnv).