ACCOFIL

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

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 about Filgrastim

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
ACCOFIL Solution for injection / infusion	European Medicines Agency (EU)	MPI, EU: SmPC

Medicine classification

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

ATC code	Group title	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)
Country: DE	Bundesinstitut für Arzneimittel und Medizinprodukte	Identifier(s): 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
Country: EE	Ravimiamet	Identifier(s): 1664849, 1664850, 1664861, 1664872, 1706363, 1706374, 1706396, 1706408, 1735837, 1735848, 1887767, 1887778, 1887789, 1887790, 1887802
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 114946005, 114946008, 114946011, 114946014
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 534589, 569876
Country: FR	Base de données publique des médicaments	Identifier(s): 60812344, 68056062
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 289864, 289874, 393475, 393481
Country: IE	Health Products Regulatory Authority	Identifier(s): 88568, 88569
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 8438, 8439
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 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
Country: NL	Z-Index G-Standaard	Identifier(s): 14165082
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 41831, 41858
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100327318, 100327324
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W65658001, W65658002, W65659001, W65659002, W67882001, W67883001
Country: TN	Direction de la Pharmacie et du Médicament	Identifier(s): 16923101H, 16923102H