ACCOFIL

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

Active ingredients

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

1	Filgrastim UNII PVI5M0M1GW - FILGRASTIM
	Filgrastim causes marked increases in peripheral blood neutrophil counts within 24 hours, with minor increases in monocytes.
	Read more about Filgrastim

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
ACCOFIL Solution for injection / 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
L03AA02	Filgrastim	L Antineoplastic and immunomodulating agents → L03 Immunostimulants → L03A Immunostimulants → L03AA Colony stimulating factors
Discover more medicines within L03AA02

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	10914422, 10914439, 12566971, 12566988, 15200124, 15200130, 15203269, 15203275, 15561980, 15569102, 15569119, 15735693, 15735701, 15747035, 15747041, 16004000, 16004017, 16584641, 16584670, 16659557, 16659563, 16659586, 16659592, 16708066, 16708126, 16782890, 16783139, 16884231, 16884248, 17524144, 17524150
EE	Ravimiamet	1664849, 1664850, 1664861, 1664872, 1706363, 1706374, 1706396, 1706408, 1735837, 1735848, 1887767, 1887778, 1887789, 1887790, 1887802
ES	Centro de información online de medicamentos de la AEMPS	114946005, 114946008, 114946011, 114946014
FI	Lääkealan turvallisuus- ja kehittämiskeskus	534589, 569876
FR	Base de données publique des médicaments	60812344, 68056062
GB	Medicines & Healthcare Products Regulatory Agency	289864, 289874, 393475, 393481
IE	Health Products Regulatory Authority	88568, 88569
IL	מִשְׂרַד הַבְּרִיאוּת	8438, 8439
LT	Valstybinė vaistų kontrolės tarnyba	1074505, 1074506, 1074507, 1074508, 1076199, 1076200, 1076201, 1076202, 1076203, 1076204, 1076205, 1076206, 1076207, 1076208, 1076209, 1076210, 1079880, 1079881, 1093024, 1093025, 1093026, 1093027, 1093028, 1093029, 1093030, 1093031, 1093032, 1093033, 1093034, 1093035, 1093036, 1093037, 1093038, 1093039, 1093040, 1093041
NL	Z-Index G-Standaard	14165082
NL	Z-Index G-Standaard, PRK	41831, 41858
PL	Rejestru Produktów Leczniczych	100327318, 100327324
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W65658001, W65658002, W65659001, W65659002, W67882001, W67883001
TN	Direction de la Pharmacie et du Médicament	16923101H, 16923102H