MIOCHOL-E

This brand name is authorized in Canada, Estonia, Finland, Ireland, Malta, New Zealand, Singapore, United Kingdom, South Africa

Active ingredients

The drug MIOCHOL-E contains one active pharmaceutical ingredient (API):

1 Acetylcholine UNII AF73293C2R - ACETYLCHOLINE CHLORIDE

Acetylcholine is a physiological neuromediator of postganglionic parasympathetic nerve fibres (muscarinic action), skeletal muscles and ganglia of the sympathetic system (nicotinic action). Read about Acetylcholine

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
MIOCHOL-E Powder and solvent for instillation solution	Medicines & Healthcare Products Regulatory Agency (GB)	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
S01EB09	Acetylcholine	S Sensory organs → S01 Ophthalmologicals → S01E Antiglaucoma preparations and miotics → S01EB Parasympathomimetics
Discover more medicines within S01EB09

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: CA	Health Products and Food Branch	Identifier(s): 02133326
Country: EE	Ravimiamet	Identifier(s): 1825343
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 019235
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 110557
Country: MT	Medicines Authority	Identifier(s): AA565/40501
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 10770
Country: SG	Health Sciences Authority	Identifier(s): 09252P
Country: ZA	Health Products Regulatory Authority	Identifier(s): 28/15.4/0506