RENFLEXIS

This brand name is authorized in Australia, Brazil, Canada, United States

Active ingredients

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

1 Infliximab
UNII B72HH48FLU - INFLIXIMAB

Infliximab is a chimeric human-murine monoclonal antibody that binds with high affinity to both soluble and transmembrane forms of TNFα but not to lymphotoxin α (TNFβ).

Read about Infliximab

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
RENFLEXIS Powder for solution for injection FDA, National Drug Code (US) MPI, US: SPL/PLR

Medicine classification

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

ATC code Group title Classification
L04AB02 Infliximab L Antineoplastic and immunomodulating agents → L04 Immunosuppressants → L04A Immunosuppressants → L04AB Tumor necrosis factor alpha (TNF-α) inhibitors
Discover more medicines within L04AB02

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 10057H, 10067W, 10184B, 10196P, 11389K, 11396T, 11399Y, 11400B, 11412P, 11423F, 11424G, 11432Q, 11445J, 11448M, 11449N, 11450P, 11459D, 11461F, 11481G, 11482H, 11483J, 11486M, 11487N, 11488P, 11489Q, 11490R, 11497D, 11498E, 11514B, 11515C, 11590B, 11595G, 11605T, 11606W, 11796W, 11797X, 5753T, 5754W, 5755X, 5756Y, 5757B, 5758C, 6397Q, 6448J, 6496X, 9612X, 9613Y, 9617E, 9654D, 9674E
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 569719010000107
Country: CA Health Products and Food Branch Identifier(s): 02470373
Country: US FDA, National Drug Code Identifier(s): 0006-4305

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