NDC 60687-449
Sevelamer Hydrochloride 800 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging 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 |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Sevelamer: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA204724
- On the market since
- Jan 22, 2020
- Package NDCs
60687-449-0160687-449-11- Official label
- DailyMed (National Library of Medicine), updated Jun 25, 2026
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