TRIAPIN

This brand name is authorized in Germany, Spain, Croatia, Ireland, United Kingdom

Active ingredients

The drug TRIAPIN contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII OL961R6O2C - FELODIPINE
 

Felodipine is a vascular selective calcium antagonist, which lowers arterial blood pressure by decreasing systemic vascular resistance. Felodipine is effective in all grades of hypertension.

 
Read more about Felodipine
2
UNII L35JN3I7SJ - RAMIPRIL
 

Ramiprilat, the active metabolite of the prodrug ramipril, inhibits the enzyme dipeptidylcarboxypeptidase I (synonyms: angiotensin-converting enzyme; kininase II). In plasma and tissue this enzyme catalyses the conversion of angiotensin I to the active vasoconstrictor substance angiotensin II, as well as the breakdown of the active vasodilator bradykinin. Reduced angiotensin II formation and inhibition of bradykinin breakdown lead to vasodilatation.

 
Read more about Ramipril

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 TRIAPIN Prolonged release tablet MPI, EU: SmPC Health Products Regulatory Authority (IE)

Medicine classification

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

ATC Group Classification
C09BB05 Ramipril and felodipine C Cardiovascular system → C09 Agents acting on the renin-angiotensin system → C09B ACE inhibitors, combinations → C09BB ACE inhibitors and calcium channel blockers
Discover more medicines within C09BB05

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 14016200, 15376840, 17836033, 17849194
ES Centro de información online de medicamentos de la AEMPS 62760
GB Medicines & Healthcare Products Regulatory Agency 140112, 146850, 374047, 38880, 40934
HR Agencija za lijekove i medicinske proizvode HR-H-458982085, HR-H-508485903
IE Health Products Regulatory Authority 50114, 50117, 50134, 50190, 72085

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