EXTAVIA

This brand name is authorized in Austria, Brazil, Canada, Cyprus, Estonia, Spain, France, Croatia, Ireland, Lithuania, Poland, United Kingdom

Active ingredients

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

1 Interferon-beta 1B recombinant
UNII TTD90R31WZ - INTERFERON BETA-1B

Interferon beta-1b has been shown to possess both antiviral and immunoregulatory activity. The mechanisms by which interferon beta-1b exerts its actions in multiple sclerosis are not clearly understood. However, it is known that the biological response-modifying properties of interferon beta-1b are mediated through its interactions with specific cell receptors found on the surface of human cells.

Read about Interferon beta-1b

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
EXTAVIA Powder and solvent for solution for injection 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
L03AB08 Interferon beta-1b L Antineoplastic and immunomodulating agents → L03 Immunostimulants → L03A Immunostimulants → L03AB Interferons
Discover more medicines within L03AB08

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): 526514120080103
Country: CA Health Products and Food Branch Identifier(s): 02337819
Country: EE Ravimiamet Identifier(s): 1361382, 1361393, 1480137, 1480148, 1480159
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 108454008
Country: FR Base de données publique des médicaments Identifier(s): 64851088
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 154037
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1070395, 1070396, 1070397, 1070398, 1070399, 1080528, 1080529
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100195390

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