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Veltassa (Patiromer) Approval Criteria: 1. An FDA approved diagnosis of hyperkalemia; and 2. A trial of a potassium-eliminating diuretic or documentation why a diuretic is not appropriate for the member; and 3. Documentation of a low potassium diet; and 4.
Veltassa (patiromer) dosage forms DosageQuantityPrice as low as 4 packets of 8.4g 1 carton $164.34 30 packets of 8.4g 1 carton $1041.00 30 packets of 16.8g 1 carton $1042.00 30 packets of 25.2g 1 carton $19.001 more row
Patients enrolled in a government health insurance program such as Medicare Part D, Medicaid, TRICARE, Veterans Health Administration, or Mi Salud are not eligible. This is not an exhaustive list of excluded government health plans. Patients are responsible for applicable taxes.
Development timeline for Veltassa DateArticle Oct 21, 2015 Approval FDA Approves Veltassa (patiromer) for Hyperkalemia Jan 5, 2015 Relypsa Announces October 21, 2015 as PDUFA Date for NDA for Patiromer for Oral Suspension3 more rows
FDA-approved indications: Lokelma and Veltassa are potassium binders indicated for the treatment of hyperkalemia (1-2).

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In order to qualify for UCB patient assistance or co-pay assistance, you must: Be a resident of the United States, the District of Columbia, or Puerto Rico. Have no insurance that provides prescription coverage, although you may still qualify if you are enrolled in a Medicare Part D plan.