SOLIQUA

This brand name is authorized in Brazil, Canada, Ecuador, Hong Kong, Japan, Singapore, Turkey, United States, South Africa

Active ingredients

The drug SOLIQUA 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  
SOLIQUA Solution for injection in pre-filled pen (SoloStar) 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: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 576720040062917, 576720040063017, 576720040063117, 576720040063217
Country: CA Health Products and Food Branch Identifier(s): 02478293
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 150-MBE-0320, 151-MBE-0320
Country: HK Department of Health Drug Office Identifier(s): 65637, 65638
Country: JP 医薬品医療機器総合機構 Identifier(s): 3969501G1023
Country: SG Health Sciences Authority Identifier(s): 15540P, 15542P
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699809951082, 8699809951099, 8699809951105, 8699809951112
Country: US FDA, National Drug Code Identifier(s): 0024-5761
Country: ZA Health Products Regulatory Authority Identifier(s): 52/32.16/0149, 52/32.16/0150

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