BLOPRESS PLUS

This brand name is authorized in Austria, Ecuador, Germany, Hong Kong SAR China, Ireland, Spain, Tunisia.

Active ingredients

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

1
UNII R85M2X0D68 - CANDESARTAN CILEXETIL
 

Candesartan is an AIIRA, selective for AT1 receptors, with tight binding to and slow dissociation from the receptor. It has no agonist activity. The antagonism of the angiotensin II (AT1) receptors results in dose related increases in plasma renin levels, angiotensin I and angiotensin II levels, and a decrease in plasma aldosterone concentration.

 
Read more about Candesartan
2
UNII 0J48LPH2TH - HYDROCHLOROTHIAZIDE
 

Hydrochlorothiazide is a diuretic with antihypertensive properties. It acts by inhibiting the renal tubular re-absorption of sodium and chloride ions, which are excreted with an accompanying volume of water. Potassium excretion is also promoted.

 
Read more about Hydrochlorothiazide

Medicine classification

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

ATC Group Classification
C09DA06 Candesartan and diuretics C Cardiovascular system → C09 Agents acting on the renin-angiotensin system → C09D Angiotensin II antagonists, combinations → C09DA Angiotensin II antagonists and diuretics
Discover more medicines within C09DA06

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 00947969, 00947975, 00947981, 01103802, 01103819, 01103825, 01301436, 05395948, 06109198, 06499845, 07288688, 07288719, 07288760, 07753369, 08884079, 08884085, 08884091, 08884116, 09294931, 09294977, 09297444, 10938316, 12650393, 16679560
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 24.354-1-01-12
ES Centro de información online de medicamentos de la AEMPS 66050, 71026
HK Department of Health Drug Office 49367, 49368
IE Health Products Regulatory Authority 63907, 63908, 63909, 63910
TN Direction de la Pharmacie et du Médicament 5063303, 5063304, 9073493, 9073494

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