BLEMAREN N

This brand name is authorized in Estonia, Lithuania.

Active ingredients

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

1
UNII 2968PHW8QP - CITRIC ACID MONOHYDRATE
 

Potassium citrate is indicated for the management of renal tubular acidosis with calcium stones, hypocitraturic calcium oxalate nephrolithiasis of any etiology, uric acid lithiasis with or without calcium stones. When potassium citrate is given orally, the metabolism of absorbed citrate produces an alkaline load. The induced alkaline load in turn increases urinary pH and raises urinary citrate by augmenting citrate clearance without measurably altering ultrafilterable serum citrate. Thus, potassium citrate therapy appears to increase urinary citrate principally by modifying the renal handling of citrate, rather than by increasing the filtered load of citrate.

 
Read more about Citric acid
2
UNII 1Q73Q2JULR - SODIUM CITRATE, UNSPECIFIED FORM
 

Sodium citrate has no relevant pharmacodynamic activity other than that caused by its alkalinity (e.g. its gastric acid neutralising capacity). Sodium citrate is a non-particulate antacid for use by mouth to prior to general anaesthesia for caesarean section.

 
Read more about Sodium citrate
3
UNII HM5Z15LEBN - POTASSIUM BICARBONATE
 
Read more about Potassium bicarbonate

Medicine classification

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

ATC Group Classification
G04BC Urinary concrement solvents G Genito urinary system and sex hormones → G04 Urologicals → G04B Other urologicals, incl. antispasmodics
Discover more medicines within G04BC

Authorization and marketing

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

Country Identification scheme Identifier(s)
EE Ravimiamet 1322693, 1781209, 1828986
LT Valstybinė vaistų kontrolės tarnyba 1012673

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