NDC 0904-7209
sevelamer hydrochloride 800 mg tablet, film coated
On the label: Major Pharmaceuticals. It's repackaged: Major Pharmaceuticals rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-447.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Dhar, India | Makes it and tests it | Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action |
Product details
- Generic drug
- Sevelamer: every company that makes it
- Form
- tablet, film coated, parenteral
- Strength
- 800 mg
- Approval
- ANDA ANDA204724
- On the market since
- Aug 19, 2024
- Package NDCs
0904-7209-06- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2026
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