LEUSTATIN

This brand name is authorized in Australia, Brazil, Japan, Netherlands, New Zealand, South Africa, Spain.

Active ingredients

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

1
UNII 47M74X9YT5 - CLADRIBINE
 

Cladribine is a nucleoside analogue of deoxyadenosine. In resting cells cladribine causes DNA single-strand breaks, rapid nicotinamide adenine dinucleotide consumption, ATP depletion and cell death.

 
Read more about Cladribine

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
L01BB04 Cladribine L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01B Antimetabolites → L01BB Purine analogues
Discover more medicines within L01BB04

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 4326Q, 7225G
BR Câmara de Regulação do Mercado de Medicamentos 514501902157315
ES Centro de información online de medicamentos de la AEMPS 61380
JP 医薬品医療機器総合機構 4291408A1021
NL Z-Index G-Standaard 13927280
NL Z-Index G-Standaard, PRK 41785
NZ Medicines and Medical Devices Safety Authority 7163
ZA Health Products Regulatory Authority 29/26/0404

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