MAVENCLAD

This brand name is authorized in United States. It is also authorized in Australia, Austria, Brazil, Canada, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, Spain, Turkey, UK.

Active ingredients

The drug MAVENCLAD 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

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 MAVENCLAD Tablet MPI, EU: SmPC European Medicines Agency (EU)

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
L04AA40 L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AA Selective immunosuppressants
Discover more medicines within L04AA40

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 11603Q, 11604R, 11611D
BR Câmara de Regulação do Mercado de Medicamentos 525420020051407, 525420020051507, 525420020051607
CA Health Products and Food Branch 02470179
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 4683-MEE-0419
EE Ravimiamet 1752443, 1752454, 1752465, 1752476, 1752487, 1752498
ES Centro de información online de medicamentos de la AEMPS 1171212001
FI Lääkealan turvallisuus- ja kehittämiskeskus 130242, 137721, 155121
FR Base de données publique des médicaments 65820786
GB Medicines & Healthcare Products Regulatory Agency 347911, 347912, 347913
HK Department of Health Drug Office 65910
IE Health Products Regulatory Authority 88966, 88967, 88968
IL מִשְׂרַד הַבְּרִיאוּת 8148, 8149, 8150
IT Agenzia del Farmaco 045615010, 045615022, 045615034, 045615046, 045615059, 045615061
LT Valstybinė vaistų kontrolės tarnyba 1083745, 1083746, 1083747, 1083748, 1083749, 1083750
NZ Medicines and Medical Devices Safety Authority 20042
PL Rejestru Produktów Leczniczych 100393522
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W64663001, W64663002, W64663003, W64663004, W64663005, W64663006
SG Health Sciences Authority 15691P
TR İlaç ve Tıbbi Cihaz Kurumu 8699808090409, 8699808090416, 8699808090423, 8699808090430, 8699808090447, 8699808090454
US FDA, National Drug Code 44087-4000

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