PROCORALAN

This brand name is authorized in Austria, Brazil, Cyprus, Germany, Ecuador, Estonia, Spain, Finland, France, Croatia, Ireland, Italy, Lithuania, Mexico, Netherlands, Poland, Tunisia, United Kingdom

Active ingredients

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

1 Ivabradine UNII TP19837BZK - IVABRADINE HYDROCHLORIDE

Ivabradine is a pure heart rate lowering agent, acting by selective and specific inhibition of the cardiac pacemaker If current that controls the spontaneous diastolic depolarisation in the sinus node and regulates heart rate. The cardiac effects are specific to the sinus node with no effect on intra-atrial, atrioventricular or intraventricular conduction times, nor on myocardial contractility or ventricular repolarisation. Read about Ivabradine

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
PROCORALAN 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
C01EB17	Ivabradine	C Cardiovascular system → C01 Cardiac therapy → C01E Other cardiac preparations → C01EB Other cardiac preparations
Discover more medicines within C01EB17

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): 531302101111218, 531302102118216, 531302103114214, 531302104110212
Country: DE	Bundesinstitut für Arzneimittel und Medizinprodukte	Identifier(s): 00434721, 00434738, 00673087, 01688122, 01689110, 02256778, 03879151, 03879814, 03880556, 03880579, 05389310, 06441403, 06441426, 07577754, 10004795, 10004803, 10004826, 10130850, 10203218, 10321053, 10321076, 10321082, 10402426, 10526051, 10554515, 10554538, 11214170, 11226799, 11258210, 11542595, 12381295, 12389279, 13862513, 15266301, 15619774, 16031681, 16031698, 17368968, 17421421
Country: EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	Identifier(s): 27.819-11-07, 27.872-10-07
Country: EE	Ravimiamet	Identifier(s): 1219463, 1219474, 1219485, 1219496, 1219508, 1219519, 1219520, 1219531, 1219542, 1219553, 1219564, 1219575, 1219586, 1219597
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 05316003, 05316003IP, 05316003IP1, 05316010, 05316010IP, 05316010IP1, 05316010IP2
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 041086, 041096, 041105, 041114
Country: FR	Base de données publique des médicaments	Identifier(s): 61952527, 63501124
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 375319, 381637, 381639, 98303, 98306
Country: IE	Health Products Regulatory Authority	Identifier(s): 42703, 42704, 42706, 42710, 42720, 42721, 42725, 42774
Country: IT	Agenzia del Farmaco	Identifier(s): 037061013, 037061025, 037061037, 037061049, 037061052, 037061064, 037061076, 037061088, 037061090, 037061102, 037061114, 037061126, 037061138, 037061140
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1030448, 1030449, 1030450, 1030451, 1030452, 1030453, 1030454, 1030455, 1030456, 1030457, 1030458, 1030459, 1030460, 1030461
Country: MX	Comisión Federal para la Protección contra Riesgos Sanitarios	Identifier(s): 204M2007
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 198161, 198188
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100147059, 100147065
Country: TN	Direction de la Pharmacie et du Médicament	Identifier(s): 6353171, 6353172