GLYPRESSIN

This brand name is authorized in Brazil, Croatia, Ecuador, Estonia, Finland, Hong Kong SAR China, Ireland, Israel, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey, UK.

Active ingredients

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

1
UNII 4U092XZF0K - TERLIPRESSIN ACETATE
 

Terlipressin inhibits portal hypertension with simultaneous reduction of blood circulation in portal vessels. Terlipressin contracts smooth oesophageal muscle with consecutive compression of oesophageal varices.

 
Read more about Terlipressin

Medicine classification

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

ATC Group Classification
H01BA04 Terlipressin H Systemic hormonal preparations, excl. Sex hormones and insulins → H01 Pituitary and hypothalamic hormones and analogues → H01B Posterior pituitary lobe hormones → H01BA Vasopressin and analogues
Discover more medicines within H01BA04

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 521400302157318, 521418020006303
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 46-MEE-0114
EE Ravimiamet 1186095, 1480441
ES Centro de información online de medicamentos de la AEMPS 61412, 72359
FI Lääkealan turvallisuus- ja kehittämiskeskus 031942, 088230
GB Medicines & Healthcare Products Regulatory Agency 180249, 48250
HK Department of Health Drug Office 36916, 61791
HR Agencija za lijekove i medicinske proizvode HR-H-413434003
IL מִשְׂרַד הַבְּרִיאוּת 6871
LT Valstybinė vaistų kontrolės tarnyba 1019805, 1054751
NL Z-Index G-Standaard 13487337
NL Z-Index G-Standaard, PRK 90301
NZ Medicines and Medical Devices Safety Authority 14932
PL Rejestru Produktów Leczniczych 100147770, 100238684
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W43555001, W67158001
SG Health Sciences Authority 07783P, 14244P
TN Direction de la Pharmacie et du Médicament 12883011H
TR İlaç ve Tıbbi Cihaz Kurumu 8697621750364, 8697621790087
ZA Health Products Regulatory Authority 43/21.13/0829

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