NDC 69367-423
Sevelamer Carbonate 800 mg tablet, film coated
On the label: Westminster Pharmaceuticals, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceutical Laboratories Inc. | Zhunan Township, Taiwan | Makes it, tests it and packages it | Problems found, fixed voluntarilyJul 21, 2025 · 7 inspections |
Product details
- Generic drug
- Sevelamer: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA200959
- On the market since
- Sep 23, 2025
- Package NDCs
69367-423-27- Official label
- DailyMed (National Library of Medicine), updated Oct 1, 2025
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