NDC 0955-1050

Sevelamer Carbonate 800 mg tablet, film coated

On the label: Sanofi-Aventis U.S. LLC.

Ireland: 1United Kingdom: 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
Eurofins Biopharma Product Testing Ireland LimitedIrelandTests it Problems found, fixed voluntarilyMay 26, 2023 · 5 inspections
Reed-Lane, Inc.Wayne, NJ, United StatesPackages it and labels it No problems foundOct 17, 2025 · 7 inspections

Product details

Generic drug
Sevelamer: every company that makes it
Form
tablet, film coated, oral
Strength
800 mg
Approval
NDA AUTHORIZED GENERIC NDA022127
On the market since
Feb 1, 2018
Package NDCs
0955-1050-27
Official label
DailyMed (National Library of Medicine), updated Nov 25, 2025

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