NDC 0955-1052
Sevelamer Carbonate 0.8 g powder, for suspension
On the label: Sanofi-Aventis U.S. LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Genzyme Ireland Limited | Waterford, Ireland | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyFeb 25, 2022 · 7 inspections |
| HVL Pharma UK Limited | Haverhill, United Kingdom | Makes the active ingredient and tests it | Problems found, fixed voluntarilyNov 3, 2022 · 6 inspections |
| Rovi Pharma Industrial Services SA | Alcala de Henares, Spain | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2024 · 5 inspections |
| Eurofins Biopharma Product Testing Ireland Limited | Ireland | Tests it | Problems found, fixed voluntarilyMay 26, 2023 · 5 inspections |
Product details
- Generic drug
- Sevelamer: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 0.8 g
- Approval
- NDA authorized generic NDA022318
- On the market since
- Jan 1, 2018
- Package NDCs
0955-1052-010955-1052-90- Official label
- DailyMed (National Library of Medicine), updated Nov 25, 2025
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