FAMPYRA

This brand name is authorized in Austria, Brazil, Canada, Cyprus, Estonia, Spain, Finland, France, Croatia, Ireland, Israel, Lithuania, Netherlands, New Zealand, Poland, Romania, Turkey

Active ingredients

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

1 Fampridine UNII BH3B64OKL9 - DALFAMPRIDINE

Fampridine is a potassium channel blocker. By blocking potassium channels, fampridine reduces the leakage of ionic current through these channels, thereby prolonging repolarization and thus enhancing action potential formation in demyelinated axons and neurological function. Read about Fampridine

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
FAMPYRA Prolonged-release tablets	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
N07XX07	Fampridine	N Nervous system → N07 Other nervous system drugs → N07X Other nervous system drugs → N07XX Other nervous system drugs
Discover more medicines within N07XX07

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: BR	Câmara de Regulação do Mercado de Medicamentos	Identifier(s): 538313110000302, 538313110000402, 538320120003007
Country: CA	Health Products and Food Branch	Identifier(s): 02379910
Country: EE	Ravimiamet	Identifier(s): 1536948, 1536959, 1880557, 1880614
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 11699003, 11699004
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 056308, 086142
Country: FR	Base de données publique des médicaments	Identifier(s): 62483787
Country: IE	Health Products Regulatory Authority	Identifier(s): 32652
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 6918
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1061715, 1061716, 1063753, 1063754
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 101826
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 14413
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100296374
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W65149001, W65149002, W65149003, W65149004
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8699783030018, 8699783030025