LOKELMA

This brand name is authorized in Austria, Canada, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Italy, Japan, Lithuania, Netherlands, Poland, Romania, United Kingdom, United States

Active ingredients

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

1 Sodium zirconium cyclosilicate
UNII D652ZWF066 - SODIUM ZIRCONIUM CYCLOSILICATE

Sodium zirconium cyclosilicate is a non-absorbed, non-polymer inorganic powder with a uniform micropore structure that preferentially captures potassium in exchange for hydrogen and sodium cations. Sodium zirconium cyclosilicate captures potassium throughout the entire gastrointestinal (GI) tract and reduces the concentration of free potassium in the GI lumen, thereby lowering serum potassium levels and increasing faecal potassium excretion to resolve hyperkalaemia.

Read about Sodium zirconium cyclosilicate

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
LOKELMA Powder for oral suspension FDA, National Drug Code (US) MPI, US: SPL/PLR

Medicine classification

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

ATC code Group title Classification
V03AE10 V Various → V03 All other therapeutic products → V03A All other therapeutic products → V03AE Drugs for treatment of hyperkalemia and hyperphosphatemia
Discover more medicines within V03AE10

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02490714, 02490722
Country: EE Ravimiamet Identifier(s): 1767573, 1767584, 1767595, 1767607, 1792841, 1792852
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1171173002, 1171173004
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 171874, 580788
Country: FR Base de données publique des médicaments Identifier(s): 64247885, 64737437
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 370618, 370624, 370626
Country: HK Department of Health Drug Office Identifier(s): 66489, 66490
Country: IT Agenzia del Farmaco Identifier(s): 046335016, 046335028, 046335030, 046335042, 046335055, 046335067, 046335079, 046335081, 046335093, 046335105, 046335117, 046335129
Country: JP 医薬品医療機器総合機構 Identifier(s): 2190040B1020, 2190040B2027
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1085278, 1085279, 1085280, 1085281, 1085819, 1085820, 1088657, 1088658, 1088659, 1088660, 1088661, 1088662
Country: NL Z-Index G-Standaard, PRK Identifier(s): 198498, 198501
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100423163, 100423170
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W65518001, W65519001
Country: US FDA, National Drug Code Identifier(s): 0310-1105, 0310-1110

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