Sodium Zirconium Cyclosilicate Generics 5g, 7g,10g sachets Suppliers & Bulk Manufacturers
Available Forms: Powder for oral suspension
Available Strengths: 5g, 7g,10g sachets
Reference Brands: Lokelma® (EU & US)
Category: Nephrology
Sodium Zirconium Cyclosilicate (SZC), marketed as Lokelma®, is a fast-acting, selective potassium binder used to treat hyperkalemia in CKD and heart failure patients. Approved in the EU and US, it is supplied as a powder for oral suspension in 5 g and 10 g sachets.
Product Description:
Sodium Zirconium Cyclosilicate (SZC), marketed as Lokelma®, is a novel, highly selective potassium binder used to treat hyperkalemia in patients with chronic kidney disease, heart failure, or those on RAAS inhibitors. Approved by the FDA and EMA, it offers rapid onset and sustained potassium control with excellent tolerability. Available as a powder for oral suspension in 5 g and 10 g strengths, SZC is in high demand across EU and US pharmaceutical B2B markets. Ideal for licensing, distribution, and contract manufacturing partnerships, SZC represents a valuable addition to renal and cardiovascular therapeutic portfolios in regulated international markets.
Sodium Zirconium Cyclosilicate Generics — third party manufacturing & bulk supply
Sodium Zirconium Cyclosilicate Generics 5g, 7g,10g sachets is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:
Indicative minimum order quantity
Sodium Zirconium Cyclosilicate Generics is supplied as Powder for oral suspension — a dosage form priced by order value, so the indicative MOQ is a minimum order value of USD 5,000 per product. Actual MOQ is confirmed by the allocated manufacturer against your pack presentation and destination market. See full supply terms for dossier formats, market availability and shelf life.
Manufacturers of Sodium Zirconium Cyclosilicate Generics listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.
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