SEGLUROMET

This brand name is authorized in United States. It is also authorized in Australia, Austria, Cyprus, Estonia, Finland, Ireland, Israel, Lithuania, Netherlands, Poland, Romania, Spain.

Active ingredients

The drug SEGLUROMET contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII MLU731K321 - ERTUGLIFLOZIN PIDOLATE
 

Ertugliflozin helps to lower blood glucose by making the patient pass out glucose in the urine. It does this by blocking a protein in the kidneys (called SGLT2) that normally takes glucose back into the blood from the kidneys.

 
Read more about Ertugliflozin
2
UNII 786Z46389E - METFORMIN HYDROCHLORIDE
 

Metformin is a biguanide with antihyperglycaemic effects, lowering both basal and postprandial plasma glucose. It does not stimulate insulin secretion and therefore does not produce hypoglycaemia.

 
Read more about Metformin

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 SEGLUROMET Film-coated tablet MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
A10BD23 Metformin and ertugliflozin A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10B Blood glucose lowering drugs, excl. insulins → A10BD Combinations of oral blood glucose lowering drugs
Discover more medicines within A10BD23

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 11562M, 11563N, 11564P, 11568W, 11569X, 11575F, 11581M, 11584Q
EE Ravimiamet 1767630, 1767641, 1767652, 1767663, 1767674, 1767685, 1767696, 1767708, 1767719, 1767720, 1767731, 1767742, 1767753, 1767764, 1767775, 1767786, 1767797, 1767809, 1767810, 1767821, 1767832, 1767843, 1767854, 1767865, 1767876, 1767887, 1767898, 1767900, 1777709, 1777710, 1777721, 1777732
ES Centro de información online de medicamentos de la AEMPS 1181265011, 1181265025
FI Lääkealan turvallisuus- ja kehittämiskeskus 088817, 459845, 489128, 511418
IL מִשְׂרַד הַבְּרִיאוּת 8309, 8310
LT Valstybinė vaistų kontrolės tarnyba 1085295, 1085296, 1085297, 1085298, 1085299, 1085300, 1085301, 1085302, 1085303, 1085304, 1085305, 1085306, 1085307, 1085308, 1085309, 1085310, 1085311, 1085312, 1085313, 1085314, 1085315, 1085316, 1085317, 1085318, 1085319, 1085320, 1085321, 1085322, 1086580, 1086581, 1086582, 1086583
NL Z-Index G-Standaard, PRK 167711, 167738
PL Rejestru Produktów Leczniczych 100403947, 100404668, 100404674, 100404680
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W66529001, W66529002, W66529003, W66529004, W66530001, W66530002, W66530003, W66530004
US FDA, National Drug Code 0006-5369, 0006-5370, 0006-5373, 0006-5374

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