BRALTUS

This brand name is authorized in Austria, Australia, Estonia, Spain, Croatia, Ireland, Lithuania, New Zealand, Poland, United Kingdom

Active ingredients

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

1 Tiotropium
UNII XX112XZP0J - TIOTROPIUM BROMIDE ANHYDROUS

Tiotropium is a long-acting, specific, muscarinic receptor antagonist, in clinical medicine often called an anticholinergic. By binding to the muscarinic receptors in the bronchial smooth musculature, tiotropium inhibits the cholinergic (bronchoconstrictive) effects of acetylcholine, released from parasympathetic nerve endings.

Read about Tiotropium

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
BRALTUS Inhalation powder, hard capsule 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
R03BB04 Tiotropium bromide R Respiratory system → R03 Drugs for obstructive airway diseases → R03B Other drugs for obstructive airway diseases, inhalants → R03BB Anticholinergics
Discover more medicines within R03BB04

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): 11892X
Country: EE Ravimiamet Identifier(s): 1667404, 1667415, 1667426, 1726578
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 80981
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 335950, 377161, 377438, 381209
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-818206056
Country: IE Health Products Regulatory Authority Identifier(s): 61508
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1074773, 1074774, 1074775, 1080688
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 20519
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100329620, 100423097

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