ENVARSUS

This brand name is authorized in United States. It is also authorized in Austria, Canada, Croatia, Estonia, Finland, France, Ireland, Lithuania, Netherlands, Poland, Spain, UK.

Active ingredients

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

1
UNII WM0HAQ4WNM - TACROLIMUS
 

Tacrolimus is a highly potent immunosuppressive agent. In particular, tacrolimus inhibits the formation of cytotoxic lymphocytes, which are mainly responsible for graft rejection. Tacrolimus suppresses T-cell activation and T-helper-cell dependent B-cell proliferation, as well as the formation of lymphokines (such as interleukins-2, -3, and γ-interferon) and the expression of the interleukin-2 receptor.

 
Read more about Tacrolimus

Medicine classification

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

ATC Group Classification
L04AD02 Tacrolimus L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AD Calcineurin inhibitors
Discover more medicines within L04AD02

Authorization and marketing

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

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 02485877, 02485885, 02485893
EE Ravimiamet 1661105, 1661116, 1661127, 1661138, 1661149, 1661150, 1661161, 1661172, 1661183
ES Centro de información online de medicamentos de la AEMPS 114935001, 114935004, 114935005, 114935007
FI Lääkealan turvallisuus- ja kehittämiskeskus 148850, 149842, 523227
FR Base de données publique des médicaments 64349915, 65037007, 69590806
GB Medicines & Healthcare Products Regulatory Agency 287919, 287922, 287925
IE Health Products Regulatory Authority 88551, 88552, 88553
LT Valstybinė vaistų kontrolės tarnyba 1074012, 1074013, 1074014, 1074015, 1074016, 1074017, 1074018, 1074019, 1074020
NL Z-Index G-Standaard, PRK 120030, 120049, 120057
PL Rejestru Produktów Leczniczych 100325845, 100325851, 100325868
US FDA, National Drug Code 68992-3010, 68992-3040, 68992-3075

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