REMODULIN

This brand name is authorized in United States. It is also authorized in Austria, Canada, Croatia, Estonia, Finland, France, Israel, Lithuania, Netherlands, Poland.

Active ingredients

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

1
UNII RUM6K67ESG - TREPROSTINIL
 

Treprostinil is a vasodilator that is used for the treatment of pulmonary arterial hypertension. Treprostinil is a potent oral antiplatelet agent. The major pharmacologic actions of treprostinil are direct vasodilation of pulmonary and systemic arterial vascular beds and inhibition of platelet aggregation. Other studies have shown that treprostinil causes a dose-related negative inotropic and lusitropic effect. Treprostinil had high affinity for the Prostaglandin D2 receptor (DP1), Prostaglandin E2 receptor EP2 subtype (EP2) and Prostaglandin D2 receptor (IP) receptors (Ki 4.4, 3.6 and 32 nM, respectively), low affinity for EP1 and EP4 receptors and even lower affinity for EP3, Prostaglandin F (FP) and thromboxane (TP) receptors. Treprostinil has demonstrated a unique effect on PPAR gamma, a transcription factor important in vascular pathogenesis as a mediator of proliferation, inflammation and apoptosis.

 
Read more about Treprostinil

Medicine classification

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

ATC Group Classification
B01AC21 Treprostinil B Blood and blood forming organs → B01 Antithrombotic agents → B01A Antithrombotic agents → B01AC Platelet aggregation inhibitors excl. heparin
Discover more medicines within B01AC21

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 02246552, 02246553, 02246554, 02246555
EE Ravimiamet 1186040, 1186062, 1186073, 1186084
FI Lääkealan turvallisuus- ja kehittämiskeskus 125613, 375005, 495203, 562419
FR Base de données publique des médicaments 60937287, 65213010, 66923928, 68635974
HR Agencija za lijekove i medicinske proizvode HR-H-129614933, HR-H-462568478, HR-H-696731975
IL מִשְׂרַד הַבְּרִיאוּת 6722, 6723, 6724
LT Valstybinė vaistų kontrolės tarnyba 1020206, 1020207, 1020208, 1020209
NL Z-Index G-Standaard, PRK 82465, 82473, 82481, 82503
PL Rejestru Produktów Leczniczych 100176010, 100176032, 100176049, 100176061
US FDA, National Drug Code 66302-101, 66302-102, 66302-105, 66302-110

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