SIMDAX

This brand name is authorized in Austria, Brazil, Cyprus, Estonia, Spain, Finland, Hong Kong, Croatia, Israel, Lithuania, Mexico, New Zealand, Poland, Romania, Turkey

Active ingredients

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

1 Levosimendan UNII C6T4514L4E - LEVOSIMENDAN

Levosimendan enhances the calcium sensitivity of contractile proteins by binding to cardiac troponin C in a calcium-dependent manner. Levosimendan increases the contraction force but does not impair ventricular relaxation. Read about Levosimendan

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
SIMDAX Injection	Medicines and Medical Devices Safety Authority (NZ)	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
C01CX08	Levosimendan	C Cardiovascular system → C01 Cardiac therapy → C01C Cardiac stimulants excl. cardiac glycosides → C01CX Other cardiac stimulants
Discover more medicines within C01CX08

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): 504118030060017
Country: EE	Ravimiamet	Identifier(s): 1245899, 1338623, 1661835, 1661846, 1661857, 1661868
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 64154
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 560557
Country: HK	Department of Health Drug Office	Identifier(s): 50409
Country: HR	Agencija za lijekove i medicinske proizvode	Identifier(s): HR-H-907457388
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 7913
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1090666
Country: MX	Comisión Federal para la Protección contra Riesgos Sanitarios	Identifier(s): 106M2002
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 10622
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100340023
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W56216001, W68192001
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8699228760012