NDC 59651-088
Sevelamer Hydrochloride 800 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Product details
- Generic drug
- Sevelamer: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA212599
- On the market since
- Jul 11, 2023
- Package NDCs
59651-088-18- Official label
- DailyMed (National Library of Medicine), updated Jan 24, 2024
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