SEEBRI

This brand name is authorized in Australia, Austria, Brazil, Canada, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Japan, Lithuania, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Tunisia, UK.

Active ingredients

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

1
UNII V92SO9WP2I - GLYCOPYRROLATE
 

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

Medicine classification

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

ATC Group Classification
R03BB06 R Respiratory system → R03 Drugs for obstructive airway diseases → R03B Other drugs for obstructive airway diseases, inhalants → R03BB Anticholinergics
Discover more medicines within R03BB06

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 10059K
BR Câmara de Regulação do Mercado de Medicamentos 526515030080802, 526516120087902
CA Health Products and Food Branch 02394936
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria H5590613
EE Ravimiamet 1595932, 1595943, 1595954, 1595965, 1595976, 1595987, 1718489
ES Centro de información online de medicamentos de la AEMPS 12778003
FI Lääkealan turvallisuus- ja kehittämiskeskus 426318, 453556
FR Base de données publique des médicaments 69941269
GB Medicines & Healthcare Products Regulatory Agency 214955, 315513, 375933, 379964
HK Department of Health Drug Office 62328
IE Health Products Regulatory Authority 30804
IL מִשְׂרַד הַבְּרִיאוּת 7119
IT Agenzia del Farmaco 042306011, 042306023, 042306035, 042306047, 042306050, 042306062, 042306074, 042306086
JP 医薬品医療機器総合機構 2259712G1029
LT Valstybinė vaistų kontrolės tarnyba 1067946, 1067947, 1067948, 1067949, 1067950, 1067951, 1076818, 1076819
MX Comisión Federal para la Protección contra Riesgos Sanitarios 103M2013
NL Z-Index G-Standaard, PRK 103942
NZ Medicines and Medical Devices Safety Authority 15874
PL Rejestru Produktów Leczniczych 100283667
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W64726001, W64726002, W64726003, W64726004, W64726005, W64726006
SG Health Sciences Authority 14431P
TN Direction de la Pharmacie et du Médicament 20833051
ZA Health Products Regulatory Authority 46/10.2.1/0840

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