SULIQUA

This brand name is authorized in Austria, Estonia, Finland, France, Croatia, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Romania, United Kingdom

Active ingredients

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

1 Insulin glargine
UNII 2ZM8CX04RZ - INSULIN GLARGINE

Insulin glargine is a human insulin analogue designed to have a low solubility at neutral pH. After injection, the acidic solution is neutralised leading to formation of a precipitate from which small amounts of insulin glargine are continuously released.

Read about Insulin glargine
2 Lixisenatide
UNII 74O62BB01U - LIXISENATIDE

Lixisenatide is a selective GLP-1 receptor agonist. The GLP-1 receptor is the target for native GLP-1, an endogenous incretin hormone that potentiates glucose-dependent insulin secretion from the pancreatic beta cells. Lixisenatide stimulates insulin secretion when blood glucose is increased but not at normoglycaemia, which limits the risk of hypoglycaemia. In parallel, glucagon secretion is suppressed. In case of hypoglycaemia, the rescue mechanism of glucagon secretion is preserved.

Read about Lixisenatide

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
SULIQUA Solution for injection European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
A10AE54 Insulin glargine and lixisenatide A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10A Insulins and analogues → A10AE Insulins and analogues for injection, long-acting
Discover more medicines within A10AE54

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1737019, 1737020, 1737031, 1737042, 1801077, 1801088
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 464322
Country: FR Base de données publique des médicaments Identifier(s): 62609556, 65503469
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 366184, 366208
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8094, 8095
Country: IT Agenzia del Farmaco Identifier(s): 045254012, 045254024, 045254036, 045254048, 045254051, 045254063
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1081959, 1081960, 1081961, 1081962, 1088327, 1088328
Country: NL Z-Index G-Standaard, PRK Identifier(s): 142506, 142514
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100383972, 100383989
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W69320001, W69321001

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