INCRUSE

This brand name is authorized in Austria, Australia, Canada, Cyprus, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Lithuania, Netherlands, New Zealand, Poland, Singapore, Tunisia, United Kingdom, United States

Active ingredients

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

1 Umeclidinium
UNII 7AN603V4JV - UMECLIDINIUM BROMIDE

Umeclidinium is a long acting muscarinic receptor antagonist (also referred to as an anticholinergic). It is a quinuclidine derivative that is a muscarinic receptor antagonist with activity across multiple muscarinic cholinergic receptor subtypes. Umeclidinium bromide exerts its bronchodilatory activity by competitively inhibiting the binding of acetylcholine with muscarinic cholinergic receptors on airway smooth muscle.

Read about Umeclidinium

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
INCRUSE ELLIPTA Inhalation powder, pre-dispensed 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
R03BB07 R Respiratory system → R03 Drugs for obstructive airway diseases → R03B Other drugs for obstructive airway diseases, inhalants → R03BB Anticholinergics
Discover more medicines within R03BB07

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 10187E
Country: CA Health Products and Food Branch Identifier(s): 02423596
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 664-MEE-0115
Country: EE Ravimiamet Identifier(s): 1646939, 1646940, 1646951
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 114922002
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 177512, 372536
Country: FR Base de données publique des médicaments Identifier(s): 68964304
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 275680, 374397, 376667, 379895, 381406
Country: HK Department of Health Drug Office Identifier(s): 63954
Country: IE Health Products Regulatory Authority Identifier(s): 61510
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 7556
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1073276, 1073277, 1073278
Country: NL Z-Index G-Standaard, PRK Identifier(s): 125318
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 17169
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100307439
Country: SG Health Sciences Authority Identifier(s): 14853P
Country: TN Direction de la Pharmacie et du Médicament Identifier(s): 2883041
Country: US FDA, National Drug Code Identifier(s): 0173-0873

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.