NDC 58468-0133

Renvela 800 mg tablet, film coated

On the label: Genzyme Corporation.

Ireland: 1United Kingdom: 1Spain: 1France: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Genzyme Ireland LimitedWaterford, IrelandMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyFeb 25, 2022 · 7 inspections
HVL Pharma UK LimitedHaverhill, United KingdomMakes the active ingredient and tests it Problems found, fixed voluntarilyNov 3, 2022 · 6 inspections
Rovi Pharma Industrial Services SAAlcala de Henares, SpainMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyJan 17, 2024 · 5 inspections
Sanofi Winthrop IndustrieAmbares Et Lagrave, FranceMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyNov 22, 2023 · 5 inspections
Eurofins Biopharma Product Testing Ireland LimitedIrelandTests it Problems found, fixed voluntarilyMay 26, 2023 · 5 inspections

Product details

Generic drug
Sevelamer: every company that makes it
Form
tablet, film coated, oral
Strength
800 mg
Approval
NDA NDA022127
On the market since
Aug 12, 2009
Package NDCs
58468-0133-1
Official label
DailyMed (National Library of Medicine), updated Nov 25, 2025

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