Europese Unie - Nederlands - EMA (European Medicines Agency)

bioprojet pharma - pitolisant - narcolepsie - andere medicijnen voor het zenuwstelsel - wakix is indicated in adults, adolescents and children from the age of 6 years for the treatment of narcolepsy with or without cataplexy (see also section 5.

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

tiofarma b.v. benjamin franklinstraat 5-10 3261 lw oud-beijerland - dapson 100 mg/stuk - tablet - lactose 1-water ; magnesiumstearaat (e 470b) ; maÏszetmeel ; natriumlaurilsulfaat (e 487) ; zetmeel, gepregelatineerd, - dapsone

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

hospira benelux bvba pleinlaan 17 1050 brussel (belgiË) - gemcitabinehydrochloride samenstelling overeenkomend met ; gemcitabine - concentraat voor oplossing voor infusie - natriumhydroxide (e 524) ; water voor injectie ; zoutzuur (e 507), - gemcitabine

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

novartis pharma b.v. haaksbergweg 16 1101 bx amsterdam - clofazimine 100 mg/stuk - capsule, hard - 4-methoxyacetophenone (ri) ; butylhydroxytolueen (e 321) ; citroenzuur 0-water (e 330) ; ethylvanilline ; gelatine (e 441) ; gele of witte was (e901) ; glycerol 85 per cent (e 422) ; ijzeroxide rood (e 172) ; ijzeroxide zwart (e 172) ; lecithine (e 322) ; natriumethylparahydroxybenzoaat ; natriumpropylparahydroxybenzoaat ; propyleenglycol (e 1520) ; raapzaadolie ; sojaboonolie ; sojaboonolie, gedeeltelijk gehydreerd, 4-methoxyacetophenone (ri) ; butylhydroxytolueen (e 321) ; citroenzuur 0-water (e 330) ; ethylvanilline ; gelatine (e 441) ; gele of witte was (e901) ; glycerol 85 per cent (e 422) ; ijzeroxide rood (e 172) ; ijzeroxide zwart (e 172) ; lecithine (e 322) ; natriumethylparahydroxybenzoaat ; natriumpropylparahydroxybenzoaat (e 217) ; propyleenglycol (e 1520) ; raapzaadolie ; sojaboonolie ; sojaboonolie, gedeeltelijk gehydreerd, - clofazimine

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

genzyme europe b.v. paasheuvelweg 25 1105 bp amsterdam - rifampicine 150 mg/stuk - capsule, hard - erythrosine (e 127) ; gelatine (e 441) ; indigokarmijn (e 132) ; magnesiumstearaat (e 470b) ; maÏszetmeel ; titaandioxide (e 171), - rifampicin

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

genzyme europe b.v. paasheuvelweg 25 1105 bp amsterdam - rifampicine 300 mg/stuk - capsule, hard - erythrosine (e 127) ; gelatine (e 441) ; indigokarmijn (e 132) ; magnesiumstearaat (e 470b) ; maÏszetmeel ; titaandioxide (e 171), - rifampicin

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

genzyme europe b.v. paasheuvelweg 25 1105 bp amsterdam - rifampicine 600 mg/stuk - poeder en oplosmiddel voor oplossing voor infusie - natriumformaldehydesulfoxylaat ; natriumhydroxide (e 524) ; stikstof (head space) (e 941) ; water, gezuiverd, - rifampicin

Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

genzyme europe b.v. paasheuvelweg 25 1105 bp amsterdam - rifampicine 20 mg/ml - suspensie voor oraal gebruik - agar ; diethanolamine (ri) ; kaliumsorbaat (e 202) ; methylparahydroxybenzoaat (e 218) ; natriummetabisulfiet (e 223) ; polysorbaat 80 (e 433) ; propylparahydroxybenzoaat ; raspberry flavour no. 5 (ri) ; saccharoide (e 954) ; saccharose ; water, gezuiverd, agar ; diethanolamine (ri) ; kaliumsorbaat (e 202) ; methylparahydroxybenzoaat (e 218) ; natriummetabisulfiet (e 223) ; polysorbaat 80 (e 433) ; propylparahydroxybenzoaat (e 216) ; raspberry flavour no. 5 (ri) ; saccharoide (e 954) ; saccharose ; water, gezuiverd, - rifampicin

Europese Unie - Nederlands - EMA (European Medicines Agency)

eli lilly nederland b.v. - abemaciclib - neoplasmata van de borst - antineoplastische middelen - early breast cancerverzenios in combination with endocrine therapy is indicated for the adjuvant treatment of adult patients with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative, node positive early breast cancer at high risk of recurrence (see section 5. in pre or perimenopausal women, aromatase inhibitor endocrine therapy should be combined with a luteinising hormone-releasing hormone (lhrh) agonist. advanced or metastatic breast cancerverzenios is indicated for the treatment of women with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant as initial endocrine-based therapy, or in women who have received prior endocrine therapy. in pre- or perimenopausal women, the endocrine therapy should be combined with a lhrh agonist.

Europese Unie - Nederlands - EMA (European Medicines Agency)

eli lilly nederland b.v. - selpercatinib - carcinoma, non-small-cell lung; thyroid neoplasms - antineoplastische middelen - retsevmo as monotherapy is indicated for the treatment of adults and adolescents 12 years and older with advanced ret-mutant medullary thyroid cancer (mtc)advanced ret fusion-positive non-small cell lung cancer (nsclc) not previously treated with a ret inhibitoradvanced ret fusion-positive thyroid cancer who require systematic therapy following prior treatment.