Ambroxol Hydrochloride Unither Pharmaceuticals 30 mg/5 ml Lösung zum Einnehmen Belgija - njemački - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

ambroxol hydrochloride unither pharmaceuticals 30 mg/5 ml lösung zum einnehmen

unither pharmaceuticals - ambroxol hydrochloride - lösung zum einnehmen - 30 mg/5 ml - ambroxol hydrochloride 6 mg/ml - ambroxol

Tamsulosin Hydrochloride Synthon 0,4 mg Hartkapsel mit veränderter Wirkstofffreisetzung Belgija - njemački - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

tamsulosin hydrochloride synthon 0,4 mg hartkapsel mit veränderter wirkstofffreisetzung

synthon - tamsulosin hydrochloride - hartkapsel mit veränderter wirkstofffreisetzung - 0,4 mg - tamsulosin hydrochloride 0.4 mg - tamsulosin

Levamisole Hydrochloride 80 % Kela Pulver zum Einnehmen Belgija - njemački - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

levamisole hydrochloride 80 % kela pulver zum einnehmen

kela - levamisole hydrochloride - pulver zum einnehmen - levamisole hydrochloride 800 mg/g - levamisole - schwein

Sitagliptin / Metformin hydrochloride Accord Europska Unija - njemački - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride accord

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - diabetes mellitus, typ 2 - drogen bei diabetes verwendet - for adult patients with type 2 diabetes mellitus:it is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. it is indicated in combination with a sulphonylurea (i. , dreifach-kombinationstherapie) als ergänzung zu diät und bewegung bei patienten, die unzureichend kontrolliert auf ihren maximalen tolerierten dosis von metformin und sulphonylurea. it is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparγ agonist. it is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

Segluromet Europska Unija - njemački - EMA (European Medicines Agency)

segluromet

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - diabetes mellitus, typ 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.

Tamsulosine Hydrochloride Yamanouchi Pharma 0,4 mg Hartkapsel mit veränderter Wirkstofffreisetzung Belgija - njemački - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

tamsulosine hydrochloride yamanouchi pharma 0,4 mg hartkapsel mit veränderter wirkstofffreisetzung

pi pharma - tamsulosin hydrochloride - hartkapsel mit veränderter wirkstofffreisetzung - 0,4 mg - tamsulosin hydrochloride 0.4 mg - tamsulosin

Icandra (previously Vildagliptin / metformin hydrochloride Novartis) Europska Unija - njemački - EMA (European Medicines Agency)

icandra (previously vildagliptin / metformin hydrochloride novartis)

novartis europharm limited - vildagliptin, metformin-hydrochlorid - diabetes mellitus, typ 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - icandra is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 und 5. 1 für verfügbare daten zu verschiedenen kombinationen).

Anafranil 25 mg/2 ml Injektionslösung Belgija - njemački - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

anafranil 25 mg/2 ml injektionslösung

alfasigma - clomipramine hydrochloride - injektionslösung - 25 mg/2 ml - clomipramine hydrochloride 25 mg - clomipramine

Sapropterin Dipharma Europska Unija - njemački - EMA (European Medicines Agency)

sapropterin dipharma

dipharma arzneimittel gmbh - sapropterin dihydrochloride - phenylketonurien - anderen verdauungstrakt und stoffwechsel-produkte, - 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.

Scemblix Europska Unija - njemački - EMA (European Medicines Agency)

scemblix

novartis europharm limited - asciminib hydrochloride - leukämie, myeloisch, chronisch, bcr-abl positiv - antineoplastische mittel - scemblix is indicated for the treatment of adult patients with philadelphia chromosome positive chronic myeloid leukaemia in chronic phase (ph+ cml cp) previously treated with two or more tyrosine kinase inhibitors (see section 5.