BRINTELLIX

This brand name is authorized in Austria, Brazil, Cyprus, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Ireland, Israel, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, United Kingdom, South Africa

Active ingredients

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

1 Vortioxetine
UNII TKS641KOAY - VORTIOXETINE HYDROBROMIDE

Vortioxetine is a 5-HT3, 5-HT7, and 5-HT1D receptor antagonist, 5-HT1B receptor partial agonist, 5-HT1A receptor agonist and inhibitor of the 5-HT transporter, leading to modulation of neurotransmission in several systems, including predominantly the serotonin but probably also the norepinephrine, dopamine, histamine, acetylcholine, GABA and glutamate systems. This multimodal activity is considered responsible for the antidepressant and anxiolytic-like effects and the improvement of cognitive function, learning and memory observed with vortioxetine in animal studies.

Read about Vortioxetine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
BRINTELLIX Film-coated tablet 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
N06AX26 N Nervous system → N06 Psychoanaleptics → N06A Antidepressants → N06AX Other antidepressants
Discover more medicines within N06AX26

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 524216010002902, 524216010003002, 524216010003202, 524216010003302, 524216010003402, 524219050003902, 524219050004002, 524219050004102, 524220120005007
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 319-MEE-0514, 324-MEE-0614, 369-MEE-0614, 401-MEE-0714
Country: EE Ravimiamet Identifier(s): 1637377, 1637388, 1637399, 1637401, 1637412, 1637423, 1637434, 1637445, 1637456, 1637467, 1637478, 1637489, 1637490, 1637502, 1637513, 1637524, 1637535, 1637546, 1637557, 1637568, 1637579, 1637580, 1637591, 1637603, 1637614, 1637625, 1637636, 1637647, 1637658, 1637726, 1674097, 1674132, 1674143
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 113891002, 113891010, 113891019, 113891028, 113891036
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 025927, 088558, 136653, 172592, 194302, 402807, 495757, 499920
Country: FR Base de données publique des médicaments Identifier(s): 60316362, 61439909, 62792157, 68562572
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 302476, 302479, 302482, 374311, 374313, 376222, 376224, 381219, 381221
Country: HK Department of Health Drug Office Identifier(s): 63599, 63600, 63601
Country: IE Health Products Regulatory Authority Identifier(s): 30110, 30123, 30258, 30307
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 7724, 7725, 7726, 7727
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1072508, 1072509, 1072510, 1072511, 1072512, 1072513, 1072514, 1072515, 1072516, 1072517, 1072518, 1072519, 1072520, 1072521, 1072522, 1072523, 1072524, 1072525, 1072526, 1072527, 1072528, 1072529, 1072530, 1072531, 1072532, 1072533, 1072534, 1072535, 1072536, 1072537, 1072538, 1072539, 1072540, 1072541, 1072542, 1072543, 1075155, 1075156, 1075157, 1075158
Country: NL Z-Index G-Standaard, PRK Identifier(s): 120731, 120758, 120766, 120952
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 20574, 20575, 20576, 20577
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100317047, 100317337, 100317350, 100317366, 100317372
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W60935001, W60998001, W60999001
Country: SG Health Sciences Authority Identifier(s): 14665P, 14666P, 14667P
Country: ZA Health Products Regulatory Authority Identifier(s): 48/1.2/0429, 48/1.2/0430, 48/1.2/0431, 48/1.2/0432

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