Zynrelef Europäische Union - Niederländisch - EMA (European Medicines Agency)

zynrelef

heron therapeutics, b.v. - bupivacaine, meloxicam - pijn, postoperatieve - anesthetica - zynrelef is indicated for treatment of somatic postoperative pain from small- to medium-sized surgical wounds in adults (see section 5.

Exparel liposomal Europäische Union - Niederländisch - EMA (European Medicines Agency)

exparel liposomal

pacira ireland limited - bupivacaine - acute pain - amides, anesthetics, local - exparel liposomal is indicated:in adults as a brachial plexus block or femoral nerve block for treatment of post-operative pain. in adults and children aged 6 years or older as a field block for treatment of somatic post-operative pain from small- to medium-sized surgical wounds.

Thiotepa Riemser Europäische Union - Niederländisch - EMA (European Medicines Agency)

thiotepa riemser

esteve pharmaceuticals gmbh - thiotepa - hematopoietic stem cell transplantation; neoplasms - antineoplastische middelen - thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients. thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients.

Solensia Europäische Union - Niederländisch - EMA (European Medicines Agency)

solensia

zoetis belgium sa - frunevetmab - pijnstillers - cats - for the alleviation of pain associated with osteoarthritis in cats.

Sapropterin Dipharma Europäische Union - Niederländisch - EMA (European Medicines Agency)

sapropterin dipharma

dipharma arzneimittel gmbh - sapropterin gluco - phenylketonurias - andere maagdarmkanaal en metabolisme producten, - sapropterin dipharma is indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with phenylketonuria (pku) who have been shown to be responsive to such treatment. sapropterin dipharma is also indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with tetrahydrobiopterin (bh4) deficiency who have been shown to be responsive to such treatment.

Pluvicto Europäische Union - Niederländisch - EMA (European Medicines Agency)

pluvicto

novartis europharm limited  - lutetium (177lu) vipivotide tetraxetan - de prostaat tumoren, castratie-resistente - therapeutische radiofarmaca - pluvicto in combination with androgen deprivation therapy (adt) with or without androgen receptor (ar) pathway inhibition is indicated for the treatment of adult patients with progressive prostate-specific membrane antigen (psma)-positive metastatic castration-resistant prostate cancer (mcrpc) who have been treated with ar pathway inhibition and taxane based chemotherapy.

Bellvalyn 150/30 microgram, filmomhulde tabletten Niederlande - Niederländisch - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

bellvalyn 150/30 microgram, filmomhulde tabletten

egis pharmaceuticals plc kereszturi ut 30-38 1106 boedapest (hongarije) - desogestrel ; ethinylestradiol - filmomhulde tablet - glyceroltriacetaat (e 1518) ; hypromellose, type 2910 (3 - 15 mpa.s) (e 464) ; ijzeroxide geel (e 172) ; indigokarmijn aluminiumlak (e 132) ; lactose 1-water ; magnesiumstearaat (e 470b) ; maÏszetmeel ; polysorbaat 80 (e 433) ; povidon k 30 (e 1201) ; siliciumdioxide (e 551) ; siliciumdioxide, gehydrateerd (e 551) ; sojaolie, gezuiverd ; stearinezuur (e 570) ; titaandioxide (e 171) ; tocoferol, d-alfa (e 307), - desogestrel and ethinylestradiol

Drospirenon/Ethinylestradiol 3/0,02 mg 24+4 Theramex, filmomhulde tabletten Niederlande - Niederländisch - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

drospirenon/ethinylestradiol 3/0,02 mg 24+4 theramex, filmomhulde tabletten

theramex ireland limited 3rd floor, kilmore house, park lane, spencer dock d01 ye64 dublin 1 (ierland) - drospirenon 3 mg/stuk ; ethinylestradiol 0,02 mg/stuk - filmomhulde tablet - croscarmellose natrium (e 468) ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; ijzeroxide zwart (e 172) ; lactose 0-water ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; maÏszetmeel, gepregelatineerd ; polysorbaat 80 (e 433) ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171), croscarmellose natrium (e 468) ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; ijzeroxide zwart (e 172) ; lactose 0-water ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; maÏszetmeel, gepregelatineerd ; polysorbaat 80 (e 433) ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171), - drospirenone and ethinylestradiol

Femilux 3 mg/0,02 mg filmomhulde tabletten Niederlande - Niederländisch - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

femilux 3 mg/0,02 mg filmomhulde tabletten

egis pharmaceuticals plc kereszturi ut 30-38 1106 boedapest (hongarije) - drospirenon 3 mg/stuk ; ethinylestradiol 0,02 mg/stuk - filmomhulde tablet - croscarmellose natrium (e 468) ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; ijzeroxide zwart (e 172) ; lactose 0-water ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; maÏszetmeel, gepregelatineerd ; polysorbaat 80 (e 433) ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171), croscarmellose natrium (e 468) ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; ijzeroxide zwart (e 172) ; lactose 0-water ; lactose 1-water ; macrogol 3350 ; magnesiumstearaat (e 470b) ; maÏszetmeel, gepregelatineerd ; polysorbaat 80 (e 433) ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171), - drospirenone and ethinylestradiol

Etonogestrel/Ethinylestradiol Leon Farma 0,120 mg/0,015 mg per 24 uur, hulpmiddel voor vaginaal gebruik Niederlande - Niederländisch - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

etonogestrel/ethinylestradiol leon farma 0,120 mg/0,015 mg per 24 uur, hulpmiddel voor vaginaal gebruik

laboratorios leon farma, s.a. c/la vallina s/n, pol. ind. 24008 navatejera (spanje) - ethinylestradiol 3,5 mg/stuk ; etonogestrel 11 mg/stuk - hulpmiddel voor vaginaal gebruik - copolymeer van ethyleen-vinylacetaat (28 pct. vinylacetaat) ; polyuretaan, - vaginal ring with progestogen and estrogen