ROLUFTA

This brand name is authorized in Austria, Croatia, Estonia, France, Ireland, Italy, Lithuania, Poland, Spain, UK.

Active ingredients

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

1
UNII GE2T1418SV - UMECLIDINIUM
 

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 more about Umeclidinium

Medicine classification

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

ATC Group 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)
EE Ravimiamet 1742071, 1742082, 1742093
ES Centro de información online de medicamentos de la AEMPS 1171174002
FR Base de données publique des médicaments 67728692
GB Medicines & Healthcare Products Regulatory Agency 391678
IT Agenzia del Farmaco 045321015, 045321027, 045321039
LT Valstybinė vaistų kontrolės tarnyba 1082483, 1082484, 1082485
PL Rejestru Produktów Leczniczych 100387119

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