MIRVASO

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

Active ingredients

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

1 Brimonidine
UNII 4S9CL2DY2H - BRIMONIDINE TARTRATE

Brimonidine is an alpha2-adrenergic receptor agonist that is 1000-fold more selective for the alpha2-adrenoceptor than the alpha1-adrenoreceptor. This selectivity results in no mydriasis and the absence of vasoconstriction in microvessels associated with human retinal xenografts.

Read about Brimonidine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
MIRVASO Gel 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
D11AX21 D Dermatologicals → D11 Other dermatological preparations → D11A Other dermatological preparations → D11AX Other dermatologicals
Discover more medicines within D11AX21

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1642463, 1642474, 1642485, 1816130, 1849653, 1849664
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 113904006
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 524981
Country: FR Base de données publique des médicaments Identifier(s): 68293613
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 241118
Country: HK Department of Health Drug Office Identifier(s): 63413
Country: IE Health Products Regulatory Authority Identifier(s): 13127
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1075473, 1075474, 1075475, 1082360
Country: NL Z-Index G-Standaard, PRK Identifier(s): 114375
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 17396
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100322657
Country: SG Health Sciences Authority Identifier(s): 14828P
Country: US FDA, National Drug Code Identifier(s): 0299-5980

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