FAMPYRA

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

Active ingredients

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

1
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 more about Fampridine

Medication package inserts

Below package inserts are available for further reading:

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

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