ONUREG

This brand name is authorized in Austria, Estonia, France, Croatia, Ireland, Israel, Italy, Lithuania, Poland, Romania, United Kingdom, United States

Active ingredients

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

1 Azacitidine
UNII M801H13NRU - AZACITIDINE

Azacitidine is believed to exert its antineoplastic effects by multiple mechanisms including cytotoxicity on abnormal haematopoietic cells in the bone marrow and hypomethylation of DNA. The cytotoxic effects of azacitidine may result from multiple mechanisms, including inhibition of DNA, RNA and protein synthesis, incorporation into RNA and DNA, and activation of DNA damage pathways.

Read about Azacitidine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
ONUREG 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
L01BC07 Azacitidine L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01B Antimetabolites → L01BC Pyrimidine analogues
Discover more medicines within L01BC07

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): 1852275, 1852286, 1852297, 1852309
Country: FR Base de données publique des médicaments Identifier(s): 64799168, 67694966
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 9047, 9048
Country: IT Agenzia del Farmaco Identifier(s): 049620014, 049620026, 049620038, 049620040
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1092904, 1092905, 1092906, 1092907
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100455330, 100455348
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W67898001, W67899001
Country: US FDA, National Drug Code Identifier(s): 59572-730, 59572-740

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