KERENDIA

This brand name is authorized in Estonia, Finland, Croatia, Israel, Italy, Japan, Lithuania, Poland, Romania, United States

Active ingredients

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

1 Finerenone UNII DE2O63YV8R - FINERENONE

Finerenone is a nonsteroidal, selective antagonist of the mineralocorticoid receptor (MR) which is activated by aldosterone and cortisol and regulates gene transcription. Its binding to the MR leads to a specific receptor-ligand complex that blocks recruitment of transcriptional coactivators implicated in the expression of pro-inflammatory and pro-fibrotic mediators. Read about Finerenone

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
KERENDIA 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
C03DA05		C Cardiovascular system → C03 Diuretics → C03D Potassium-sparing agents → C03DA Aldosterone antagonists
Discover more medicines within C03DA05

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): 1876170, 1876181, 1876192, 1876204, 1876215, 1876226, 1876237, 1876248, 1876259, 1876260, 1876271, 1876282
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 066372, 087492, 524798, 554185
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 9212, 9213
Country: IT	Agenzia del Farmaco	Identifier(s): 049927015, 049927027, 049927039, 049927041, 049927054, 049927066, 049927078, 049927080, 049927092, 049927104
Country: JP	医薬品医療機器総合機構	Identifier(s): 2190044F1020, 2190044F2027
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1094270, 1094271, 1094272, 1094273, 1094274, 1094275, 1094276, 1094277, 1094278, 1094279
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100465400, 100465424
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W69353001, W69354001
Country: US	FDA, National Drug Code	Identifier(s): 50419-540, 50419-541