Sitagliptin / Metformin hydrochloride Accord Europese Unie - Nederlands - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride accord

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - diabetes mellitus, type 2 - geneesmiddelen die worden gebruikt bij diabetes - 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. , drievoudige combinatietherapie) als aanvulling op dieet en lichaamsbeweging bij patiënten die onvoldoende gecontroleerd op hun maximale getolereerde dosis van metformine en een enz.). 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.

Vildagliptin / Metformin hydrochloride Accord Europese Unie - Nederlands - EMA (European Medicines Agency)

vildagliptin / metformin hydrochloride accord

accord healthcare s.l.u. - metformin hydrochloride, vildagliptin - diabetes mellitus, type 2 - geneesmiddelen die worden gebruikt bij diabetes - vildagliptin/metformin hydrochloride accord 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 en 5. 1 voor de beschikbare gegevens over verschillende combinaties).

Sitagliptin / Metformin hydrochloride Mylan Europese Unie - Nederlands - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride mylan

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabetes mellitus, type 2 - geneesmiddelen die worden gebruikt bij diabetes - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride mylan 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. sitagliptin/metformin hydrochloride mylan is indicated in combination with a sulphonylurea (i. , drievoudige combinatietherapie) als aanvulling op dieet en lichaamsbeweging bij patiënten die onvoldoende gecontroleerd op hun maximale getolereerde dosis van metformine en een enz.). sitagliptin/metformin hydrochloride mylan is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparg) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparg agonist. sitagliptin/metformin hydrochloride mylan 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.

Sitagliptin / Metformin hydrochloride Sun Europese Unie - Nederlands - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride sun

sun pharmaceutical industries europe b.v. - sitagliptin fumarate, metformin hydrochloride - diabetes mellitus, type 2 - geneesmiddelen die worden gebruikt bij diabetes - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride sun 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. sitagliptin/metformin hydrochloride sun is indicated in combination with a sulphonylurea (i. , drievoudige combinatietherapie) als aanvulling op dieet en lichaamsbeweging bij patiënten die onvoldoende gecontroleerd op hun maximale getolereerde dosis van metformine en een enz.). sitagliptin/metformin hydrochloride sun 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. sitagliptin/metformin hydrochloride sun 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.

Sitagliptine/Metformine hydrochloride Grindeks 50 mg/1000 mg, filmomhulde tabletten Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

sitagliptine/metformine hydrochloride grindeks 50 mg/1000 mg, filmomhulde tabletten

metforminehydrochloride 1000 mg/stuk samenstelling overeenkomend met ; metformine 779,6 mg/stuk ; sitagliptinehydrochloride 1-water 56,7 mg/stuk samenstelling overeenkomend met ; sitagliptine 50 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460) ; copolymeer van macrogol (25,0)-poly(vinyl alcohol) (75,0) ; glycerol monocaprylocapraat, type i ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; ijzeroxide zwart (e 172) ; natriumlaurilsulfaat (e 487) ; natriumstearylfumaraat ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171)

Sitagliptine/Metformine hydrochloride Grindeks 50 mg/850 mg, filmomhulde tabletten Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

sitagliptine/metformine hydrochloride grindeks 50 mg/850 mg, filmomhulde tabletten

metforminehydrochloride 850 mg/stuk samenstelling overeenkomend met ; metformine 662,7 mg/stuk ; sitagliptinehydrochloride 1-water 56,7 mg/stuk samenstelling overeenkomend met ; sitagliptine 50 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460) ; copolymeer van macrogol (25,0)-poly(vinyl alcohol) (75,0) ; glycerol monocaprylocapraat, type i ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; natriumlaurilsulfaat (e 487) ; natriumstearylfumaraat ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171)

Sitagliptine/Metformine hydrochloride Reddy 50 mg/1000 mg filmomhulde tabletten Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

sitagliptine/metformine hydrochloride reddy 50 mg/1000 mg filmomhulde tabletten

metforminehydrochloride 1000 mg/stuk samenstelling overeenkomend met ; metformine 779,6 mg/stuk ; sitagliptinehydrochloride 1-water 56,7 mg/stuk samenstelling overeenkomend met ; sitagliptine 50 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460) ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumlaurilsulfaat (e 487) ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171)

Sitagliptine/Metformine hydrochloride Reddy 50 mg/850 mg filmomhulde tabletten Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

sitagliptine/metformine hydrochloride reddy 50 mg/850 mg filmomhulde tabletten

metforminehydrochloride 850 mg/stuk samenstelling overeenkomend met ; metformine 662,7 mg/stuk ; sitagliptinehydrochloride 1-water 56,7 mg/stuk samenstelling overeenkomend met ; sitagliptine 50 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460) ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumlaurilsulfaat (e 487) ; polyvinylalcohol, gedeeltelijk gehydrolyseerd (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171)

Sitagliptine/Metformine hydrochloride Genericon 50 mg/1000 mg filmomhulde tabletten Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

sitagliptine/metformine hydrochloride genericon 50 mg/1000 mg filmomhulde tabletten

metforminehydrochloride samenstelling overeenkomend met ; metformine ; sitagliptinehydrochloride 1-water samenstelling overeenkomend met ; sitagliptine - filmomhulde tablet - cellulose, microkristallijn (e 460) ; ijzeroxide geel (e 172) ; ijzeroxide rood (e 172) ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumlaurilsulfaat (e 487) ; polyvinylalcohol (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171)

Sitagliptine/Metformine hydrochloride Genericon 50 mg/850 mg filmomhulde tabletten Nederland - Nederlands - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

sitagliptine/metformine hydrochloride genericon 50 mg/850 mg filmomhulde tabletten

metforminehydrochloride samenstelling overeenkomend met ; metformine ; sitagliptinehydrochloride 1-water samenstelling overeenkomend met ; sitagliptine - filmomhulde tablet - cellulose, microkristallijn (e 460) ; ijzeroxide rood (e 172) ; ijzeroxide zwart (e 172) ; macrogol 3350 ; magnesiumstearaat (e 470b) ; natriumlaurilsulfaat (e 487) ; polyvinylalcohol (e1203) ; povidon k 30 (e 1201) ; talk (e 553 b) ; titaandioxide (e 171)