GUTRON

This brand name is authorized in Austria, Estonia, France, Germany, Hong Kong SAR China, Netherlands, New Zealand, Poland, Romania, Singapore, Spain.

Active ingredients

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

1	Midodrine UNII 59JV96YTXV - MIDODRINE HYDROCHLORIDE
	Midodrine is the rapidly absorbed pro-drug of the pharmacologically active constituent desglymidodrine. Desglymidodrine is a sympathicomimetic with a direct and selective effect on the peripheral α1-adrenergic receptors. This α1-stimulative effect induces vasoconstriction of the venous system.
	Read more about Midodrine

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
GUTRON Tablets	MPI, EU: SmPC	European Medicines Agency (EU)

Medicine classification

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

ATC Group		Classification
C01CA17	Midodrine	C Cardiovascular system → C01 Cardiac therapy → C01C Cardiac stimulants excl. cardiac glycosides → C01CA Adrenergic and dopaminergic agents
Discover more medicines within C01CA17

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	00474583, 02067385, 02494130, 03337160, 03928470, 03928487, 04273485, 04408287, 08537107, 08537113, 08874402, 08874419, 13910927, 15888698, 15996583
EE	Ravimiamet	1100091, 1109292, 1285916, 1621482, 1667336
ES	Centro de información online de medicamentos de la AEMPS	65058
FR	Base de données publique des médicaments	61296838, 62055338, 62232411, 67210447, 69766001
HK	Department of Health Drug Office	19584
NL	Z-Index G-Standaard, PRK	50717
NZ	Medicines and Medical Devices Safety Authority	5484, 5485
PL	Rejestru Produktów Leczniczych	100027674, 100260293, 100292880, 100326135, 100346184, 100356604, 100356886, 100364182, 100369541, 100386410, 100400038, 100400452, 100425386, 100468680
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W67703001, W67703002, W67703003
SG	Health Sciences Authority	11500P