VISTABEL

This brand name is authorized in Austria, Cyprus, Estonia, Spain, Finland, France, Croatia, Ireland, Lithuania, Malta, Poland, Romania

Active ingredients

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

1 Botulinum toxin type A
UNII E211KPY694 - BOTULINUM TOXIN TYPE A

Botulinum toxin type A is a protein complex derived from Clostridium botulinum. The protein consists of type A neurotoxin and several other proteins. Under physiological conditions it is presumed that the complex dissociates and releases the pure neurotoxin. Intramuscular injection of the neurotoxin complex blocks cholinergic transport at the neuromuscular junction by preventing the release of acetylcholine. The nerve endings of the neuromuscular junction no longer respond to nerve impulses and secretion of the chemotransmitter is prevented (chemical denervation).

Read about Botulinum toxin type A

Medicine classification

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

ATC code Group title Classification
M03AX01 Botulinum toxin M Musculo-skeletal system → M03 Muscle relaxants → M03A Muscle relaxants, peripherally acting agents → M03AX Other muscle relaxants, peripherally acting agents
Discover more medicines within M03AX01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1161605, 1616015, 1783177, 1783188
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 65837
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 022250
Country: FR Base de données publique des médicaments Identifier(s): 68150775
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-430530691
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1017350, 1021234, 1086419, 1086420, 1089500, 1093214
Country: MT Medicines Authority Identifier(s): MA1304/00301
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100191959
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W69201001, W69201002, W69201003, W69201004

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