GUTRON

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

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 about Midodrine

Medication package inserts

Below package inserts are available for further reading:

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