FLIXABI

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, France, Germany, Ireland, Lithuania, Netherlands, Poland, Romania, Spain, UK.

Active ingredients

The drug FLIXABI 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 more about Infliximab

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
FLIXABI Powder for concentrate for solution for infusion	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
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)
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	11655945, 11655968, 11655974, 11655980, 12501279, 13716154, 13716160, 14162841, 14162858, 14162864, 14306458, 14306470, 14356775, 14356781, 14356798, 14357792, 15386258, 15386264, 15568321, 15568344, 15568367, 15613435, 15613441, 15890755, 15890778, 15890784, 16146496, 16236176, 16799092, 16914475, 17522323, 17522346, 17551572, 17589511, 17589528
EE	Ravimiamet	1722383, 1750430, 1750441, 1750452, 1750463
ES	Centro de información online de medicamentos de la AEMPS	1161106001
FR	Base de données publique des médicaments	69531804
GB	Medicines & Healthcare Products Regulatory Agency	330879
LT	Valstybinė vaistų kontrolės tarnyba	1080509, 1083715, 1083716, 1083717, 1083718, 1088673
NL	Z-Index G-Standaard, PRK	54542
PL	Rejestru Produktów Leczniczych	100373360
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W63431001, W63431002, W63431003, W63431004, W63431005