MIOSTAT

This brand name is authorized in United States. It is also authorized in Canada, Ecuador, Estonia, France, Hong Kong SAR China, Netherlands, New Zealand, Poland, Singapore, Turkey.

Active ingredients

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

1
UNII 8Y164V895Y - CARBACHOL
 

Carbachol is a potent cholinergic (parasympathomimetic) agent which produces constriction of the iris and ciliary body resulting in reduction in intraocular pressure (IOP).

 
Read more about Carbachol

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 MIOSTAT Solution for injection MPI, US: SPL/Old FDA, National Drug Code (US)

Medicine classification

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

ATC Group Classification
S01EB02 Carbachol S Sensory organs → S01 Ophthalmologicals → S01E Antiglaucoma preparations and miotics → S01EB Parasympathomimetics
Discover more medicines within S01EB02

Authorization and marketing

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

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 00042544
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 16.108-2-04-02
EE Ravimiamet 1111789, 1730348
FR Base de données publique des médicaments 67713498
HK Department of Health Drug Office 24136
NL Z-Index G-Standaard 13930656
NL Z-Index G-Standaard, PRK 27839
NZ Medicines and Medical Devices Safety Authority 2405
PL Rejestru Produktów Leczniczych 100044030
SG Health Sciences Authority 04572P
TR İlaç ve Tıbbi Cihaz Kurumu 8699760610189, 8699760610196
US FDA, National Drug Code 0065-0023

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