BOCOUTURE

This brand name is authorized in Austria, Croatia, Estonia, Finland, France, Ireland, Malta, Netherlands, Poland, Romania, Spain, UK.

Active ingredients

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

1	Clostridium botulinum typa-A toxin 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 more about Botulinum toxin type A

Medicine classification

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

ATC Group		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)
EE	Ravimiamet	1825196, 1825208, 1825219, 1825220, 1825231, 1825242, 1825253, 1825264
ES	Centro de información online de medicamentos de la AEMPS	72709, 81177
FI	Lääkealan turvallisuus- ja kehittämiskeskus	156748, 430448
FR	Base de données publique des médicaments	60707788, 61592762
GB	Medicines & Healthcare Products Regulatory Agency	175612, 340526
HR	Agencija za lijekove i medicinske proizvode	HR-H-089001793, HR-H-311134880
MT	Medicines Authority	MA025/00604, MA025/00605
NL	Z-Index G-Standaard	15647471
NL	Z-Index G-Standaard, PRK	115975, 95818
PL	Rejestru Produktów Leczniczych	100238164, 100376179
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W67511001, W67511002, W67511003, W67511004, W67511005, W67511006, W67511007, W67512001, W67512002, W67512003, W67512004, W67512005, W67512006, W67512007