SIALANAR

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

Active ingredients

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

1 Glycopyrronium
UNII H4S7L81L98 - CHLOROGLYCOPYRRONIUM BROMIDE

Glycopyrronium is an inhaled long-acting muscarinic receptor antagonist (anticholinergic) for once-daily maintenance bronchodilator treatment of COPD. Glycopyrronium works by blocking the bronchoconstrictor action of acetylcholine on airway smooth muscle cells, thereby dilating the airways.

Read about Glycopyrronium

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
SIALANAR Oral solution Medicines & Healthcare Products Regulatory Agency (GB) 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
A03AB02 Glycopyrronium bromide A Alimentary tract and metabolism → A03 Drugs for functional gastrointestinal disorders → A03A DRUGS FOR FUNCTIONAL BOWEL DISORDERS → A03AB Synthetic anticholinergics, quaternary ammonium compounds
Discover more medicines within A03AB02

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): 1729155, 1798139
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 171056
Country: FR Base de données publique des médicaments Identifier(s): 62719472
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 337308, 366848
Country: IE Health Products Regulatory Authority Identifier(s): 30800
Country: IT Agenzia del Farmaco Identifier(s): 045092018, 045092020
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1081083, 1087548
Country: NL Z-Index G-Standaard, PRK Identifier(s): 199109
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100377641
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W69128001, W69128002

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