How is patiromer stored?

Refrigerated at 2â8 Â°C; it can be kept at room temperature for up to 3 months.

Patiromer 8.4 g sachet bulk supplier for pharma manufacturers

Patiromer 8.4 g Sachet 8.4g Suppliers & Bulk Manufacturers

Available Forms: sachet

Available Strengths: 8.4g

Reference Brands:

Patiromer is an oral potassium binder that removes excess potassium through the gut, used for high blood potassium (hyperkalaemia) in kidney disease and in patients taking RAAS-inhibitor heart medicines. It comes as 8.4 g, 16.8 g and 25.2 g sachets mixed with water. The originator product is Veltassa; US generic entry is expected from 2027. Patent status differs by country, so we confirm what can lawfully be supplied to your destination before quoting.

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Product Description: Help decreasing serum potassium in patients with hyperkalemia

Patiromer 8.4 g Sachet — third party manufacturing & bulk supply

Patiromer 8.4 g Sachet 8.4g 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:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.

Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.

Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

Indicative minimum order quantity

Patiromer 8.4 g Sachet is supplied as sachet — an oral solid dosage form, so the indicative MOQ is 200,000 units. 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 Patiromer 8.4 g Sachet listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.

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Usually answered within 48 hours, with matched manufacturers, indicative prices and document status.

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