NDC 68180-133
Sevelamer Carbonate 800 mg tablet, film coated
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Nagpur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Product details
- Generic drug
- Sevelamer: every company that makes it
- Form
- tablet, film coated
- Strength
- 800 mg
- Approval
- ANDA ANDA204600
- On the market since
- Jan 1, 2024
- Package NDCs
68180-133-0668180-133-28- Official label
- DailyMed (National Library of Medicine), updated Jan 15, 2021
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