NDC 68151-5113
Renvela 800 mg tablet, film coated
On the label: Carilion Materials Management. It's repackaged: Carilion Materials Management rebottles it from Genzyme Corporation's NDC 58468-0130.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| 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 |
| Sanofi Winthrop Industrie | Ambares Et Lagrave, France | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyNov 22, 2023 · 5 inspections |
| Eurofins Biopharma Product Testing Ireland Limited | Ireland | Tests it | Problems found, fixed voluntarilyMay 26, 2023 · 5 inspections |
| Reed-Lane, Inc. | Wayne, NJ, United States | Packages it and labels it | No problems foundOct 17, 2025 · 7 inspections |
Repackaging site
- Carilion Materials Management, Roanoke, Virginia, United States · repackages it
Product details
- Generic drug
- Sevelamer: every company that makes it
- Form
- tablet, film coated
- Strength
- 800 mg
- Approval
- NDA NDA022127
- On the market since
- Aug 12, 2009
- Package NDCs
68151-5113-1- Official label
- DailyMed (National Library of Medicine), updated Aug 6, 2016
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