ALPHAGAN

This brand name is authorized in Austria, Australia, Brazil, Canada, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Malta, Mexico, Netherlands, New Zealand, Poland, Singapore, Tunisia, Turkey, United Kingdom, United States, South Africa

Active ingredients

The drug ALPHAGAN 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  
ALPHAGAN Eye drops, solution Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC
ALPHAGAN P Ophthalmic solution / drops FDA, National Drug Code (US) MPI, US: SPL/PLR

Medicine classification

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

ATC code Group title Classification
S01EA05 Brimonidine S Sensory organs → S01 Ophthalmologicals → S01E Antiglaucoma preparations and miotics → S01EA Sympathomimetics in glaucoma therapy
Discover more medicines within S01EA05

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): 5298W, 5534G, 5563T, 8351M
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 501000301175318, 501000302171316, 501000401171314, 501006401171313, 501016060012403
Country: CA Health Products and Food Branch Identifier(s): 02236876, 02248151
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 25.856-08-04
Country: EE Ravimiamet Identifier(s): 1238880, 1609477, 1755806
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 62010
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 174433, 174664
Country: FR Base de données publique des médicaments Identifier(s): 68451230
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 138272, 13845, 140550, 161371, 374168
Country: HK Department of Health Drug Office Identifier(s): 50368
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-063917030
Country: IE Health Products Regulatory Authority Identifier(s): 11298, 11301, 11306, 13033
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 4785
Country: IT Agenzia del Farmaco Identifier(s): 033490020, 044819011, 045282011, 045633017, 045769015
Country: MT Medicines Authority Identifier(s): MA1304/00201
Country: MX Comisión Federal para la Protección contra Riesgos Sanitarios Identifier(s): 147M98
Country: NL Z-Index G-Standaard Identifier(s): 14181150
Country: NL Z-Index G-Standaard, PRK Identifier(s): 50237
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 11926, 7798
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100100520
Country: SG Health Sciences Authority Identifier(s): 09788P, 12336P
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699490561041
Country: US FDA, National Drug Code Identifier(s): 0023-9177, 0023-9321
Country: ZA Health Products Regulatory Authority Identifier(s): A39/15.4/0202

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.