KALINOR

This brand name is authorized in Germany, Lithuania, Turkey

Active ingredients

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

1 Potassium citrate
UNII EE90ONI6FF - POTASSIUM CITRATE

Citrate and citric acid solutions are systematic and urinary alkalinizers thereby providing symptomatic relief of dysuria.

Read about Potassium citrate
2 Potassium bicarbonate
UNII HM5Z15LEBN - POTASSIUM BICARBONATE
Read about Potassium bicarbonate
3 Citric acid
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 about Citric acid

Medicine classification

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

ATC code Group title Classification
A12BA02 Potassium citrate A Alimentary tract and metabolism → A12 Mineral supplements → A12B Potassium → A12BA Potassium
Discover more medicines within A12BA02

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 01566347, 02135106, 07515598
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1006094
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699738020019, 8699738020026

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