ZIMBUS

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

Active ingredients

The drug ZIMBUS contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII RYI4401DTM - INDACATEROL ACETATE
 

Indacaterol is a partial agonist at the human beta2-adrenergic receptor with nanomolar potency. When inhaled, indacaterol acts locally in the lung as a bronchodilator. In isolated human bronchus, indacaterol has a rapid onset of action and a long duration of action.

 
Read more about Indacaterol
2
UNII A14FB57V1D - GLYCOPYRRONIUM
 

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 more about Glycopyrronium
3
UNII 04201GDN4R - MOMETASONE FUROATE
 

Mometasone is a topical glucocorticoid with local anti-inflammatory properties. It is likely that much of the mechanism for the effects of mometasone lies in its ability to inhibit the release of mediators of the inflammatory cascade.

 
Read more about Mometasone

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 ZIMBUS BREEZHALER Inhalation powder (hard capsule) MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

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

ATC Group Classification
R03AL12 R Respiratory system → R03 Drugs for obstructive airway diseases → R03A Adrenergics, inhalants → R03AL Adrenergics in combination with anticholinergics
Discover more medicines within R03AL12

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 1822069, 1822070, 1822081, 1822092, 1822104
ES Centro de información online de medicamentos de la AEMPS 1201440002
IT Agenzia del Farmaco 048917013, 048917025, 048917037, 048917049, 048917052
LT Valstybinė vaistų kontrolės tarnyba 1090765, 1090766, 1090767, 1090768, 1090769
PL Rejestru Produktów Leczniczych 100440167
ZA Health Products Regulatory Authority 54/10.2.1/0875.873, 54/10.2.1/0876.874, E/2.10/229

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