Lerdip 20 mg, filmomhulde tabletten নেদারল্যান্ডস - ডাচ - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

lerdip 20 mg, filmomhulde tabletten

recordati ireland ltd. (co. cork) raheens east ringaskiddy (ierland) - lercanidipinehydrochloride samenstelling overeenkomend met ; ; lercanidipine 18,8 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460(i)) ; hypromellose (e 464) ; ijzeroxide (type en kleur onbekend) (e 172) ; lactose 1-water ; magnesiumstearaat (e 470b) ; natriumzetmeelglycolaat ; polyethyleenglycol (e 1521) ; povidon (e 1201) ; talk (e 553 b) ; titaandioxide (e 171), cellulose, microkristallijn (e 460) ; hypromellose (e 464) ; ijzeroxide (type en kleur onbekend) (e 172) ; lactose 1-water ; magnesiumstearaat (e 470b) ; natriumzetmeelglycolaat ; polyethyleenglycol (e 1521) ; povidon (e 1201) ; talk (e 553 b) ; titaandioxide (e 171), cellulose, microkristallijn (e 460) ; hypromellose (e 464) ; ijzeroxide (type en kleur onbekend) (e 172) ; lactose 1-water ; magnesiumstearaat (e 470b) ; natriumzetmeelglycolaat (e468) ; polyethyleenglycol (e 1521) ; povidon (e 1201) ; talk (e 553 b) ; titaandioxide (e 171), - lercanidipine

Venoruton Forte 500 mg Tablet বেলজিয়াম - ডাচ - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

venoruton forte 500 mg tablet

impexeco - hydroxyethyl-o-(bèta-)-rutoside - tablet - 500 mg - hydroxyethyl-o-(bèta-)-rutoside 500 mg - troxerutin, combinations

Voluven 10 % inf. opl. i.v. বেলজিয়াম - ডাচ - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

voluven 10 % inf. opl. i.v.

fresenius kabi sa-nv - natriumchloride 4,5 g/500 ml; hydroxyethylzetmeel 50 g/500 ml - oplossing voor infusie - 10 % (100 mg/ml) - natriumchloride 9 mg/ml; hydroxyethylzetmeel 100 mg/ml - hydroxyethylstarch

Venoruton Forte 500 mg Tablet বেলজিয়াম - ডাচ - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

venoruton forte 500 mg tablet

orifarm - hydroxyethyl-o-(bèta-)-rutoside - tablet - 500 mg - hydroxyethyl-o-(bèta-)-rutoside 500 mg - troxerutin, combinations

Byooviz ইউরোপীয় ইউনিয়ন - ডাচ - EMA (European Medicines Agency)

byooviz

samsung bioepis nl b.v. - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; myopia, degenerative - ophthalmologica - 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).

Ximluci ইউরোপীয় ইউনিয়ন - ডাচ - EMA (European Medicines Agency)

ximluci

stada arzneimittel ag - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - ophthalmologica - 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).

Ranivisio ইউরোপীয় ইউনিয়ন - ডাচ - EMA (European Medicines Agency)

ranivisio

midas pharma gmbh - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - ophthalmologica - 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).

Ariclaim ইউরোপীয় ইউনিয়ন - ডাচ - EMA (European Medicines Agency)

ariclaim

eli lilly nederland b.v. - duloxetine - diabetische neuropathieën - psychoanaleptics, - behandeling van diabetische perifere neuropathische pijn. ariclaim is geïndiceerd bij volwassenen.

Duloxetine Boehringer Ingelheim ইউরোপীয় ইউনিয়ন - ডাচ - EMA (European Medicines Agency)

duloxetine boehringer ingelheim

boehringer ingelheim international gmbh - duloxetine - diabetische neuropathieën - psychoanaleptics, - behandeling van diabetische perifere neuropathische pijn bij volwassenen.

TATICA 250 mg, filmomhulde tabletten নেদারল্যান্ডস - ডাচ - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

tatica 250 mg, filmomhulde tabletten

pharos pharmaceutical oriented services ltd lesvou str. (end), thesi loggos industrial zone 14452 metamorfossi attikis (grie - abirateronacetaat 250 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460(i)) ; croscarmellose natrium (e 468) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumlaurilsulfaat ; polyvinylalcohol (e 1203) ; povidon k 30 (e 1201) ; siliciumdioxide (e 551) ; talk (e 553 b) ; titaandioxide (e 171), cellulose, microkristallijn (e 460) ; croscarmellose natrium (e 468) ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumlaurilsulfaat (e 487) ; polyvinylalcohol (e1203) ; povidon k 30 (e 1201) ; siliciumdioxide (e 551) ; talk (e 553 b) ; titaandioxide (e 171)