LONSURF

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, Japan, Lithuania, Netherlands, Poland, Romania, Singapore, Spain, UK.

Active ingredients

The drug LONSURF contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII RMW9V5RW38 - TRIFLURIDINE
 
Read more about Trifluridine
2
UNII 4H59KLQ0A4 - TIPIRACIL HYDROCHLORIDE
 

Tipiracil helps maintain the blood concentration of trifluridine by inhibiting the enzyme thymidine phosphorylase which metabolizes trifluridine.

 
Read more about Tipiracil

Medicine classification

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

ATC Group Classification
L01BC59 L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01B Antimetabolites → L01BC Pyrimidine analogues
Discover more medicines within L01BC59

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 11507P, 11524M, 12033H, 12056M
BR Câmara de Regulação do Mercado de Medicamentos 531320090011107, 531320090011207, 531320090011307, 531320090011407
CA Health Products and Food Branch 02472104, 02472112
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 5189-MEE-0620, 5190-MEE-0620
EE Ravimiamet 1716319, 1716320, 1716331, 1716342, 1716353, 1716364
ES Centro de información online de medicamentos de la AEMPS 1161096001, 1161096003, 1161096004, 1161096006
FI Lääkealan turvallisuus- ja kehittämiskeskus 057979, 158698, 389330, 516182
FR Base de données publique des médicaments 65185956, 69681469
GB Medicines & Healthcare Products Regulatory Agency 329756, 329757, 329761, 329762
HK Department of Health Drug Office 65360, 65361
IE Health Products Regulatory Authority 88850, 88851, 88852, 88853
IL מִשְׂרַד הַבְּרִיאוּת 8802, 8803
IT Agenzia del Farmaco 044856019, 044856021, 044856033, 044856045, 044856058, 044856060
JP 医薬品医療機器総合機構 4299100F1026, 4299100F2022
LT Valstybinė vaistų kontrolės tarnyba 1080198, 1080199, 1080200, 1080201, 1080202, 1080203
NL Z-Index G-Standaard, PRK 137510, 137529
PL Rejestru Produktów Leczniczych 100370700, 100370716
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W63841001, W63841002, W63842001, W63842002
SG Health Sciences Authority 15491P, 15494P
US FDA, National Drug Code 64842-1020, 64842-1025

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