ELMIRON

This brand name is authorized in Austria, Canada, Estonia, France, Croatia, Ireland, Italy, Lithuania, Netherlands, Poland, Turkey, United Kingdom, United States

Active ingredients

The drug ELMIRON contains one active pharmaceutical ingredient (API):

1 Pentosan polysulfate
UNII 914032762Y - PENTOSAN POLYSULFATE SODIUM

The hypothetic mechanism of action of pentosan polysulfate includes a local effect in the bladder after systemic administration and excretion into the urine by binding of glycosaminoglycans to the deficient mucous of the bladder. It is hypothesized, that a potential barrier function of pentosan polysulfate instead of the damaged urothelial mucus might play a role as well the antiinflammatory activity of pentosan polysulfate sodium.

Read about Pentosan polysulfate

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
ELMIRON Hard capsule 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
G04BX15 Pentosan polysulfate sodium G Genito urinary system and sex hormones → G04 Urologicals → G04B Other urologicals, incl. antispasmodics → G04BX Other urologicals
Discover more medicines within G04BX15

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02029448
Country: EE Ravimiamet Identifier(s): 1747560, 1789195, 1789207, 1863413
Country: FR Base de données publique des médicaments Identifier(s): 60027685
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 356548, 357500
Country: IT Agenzia del Farmaco Identifier(s): 045487016, 045487028, 045487030
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1083165, 1083166, 1088298
Country: NL Z-Index G-Standaard, PRK Identifier(s): 93904
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100391865
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699771000887
Country: US FDA, National Drug Code Identifier(s): 50458-098

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