NDC 71205-966
Sevelamer Carbonate 800 mg tablet, film coated
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from TWi Pharmaceuticals, Inc.'s NDC 24979-186.
Where the pills inside were 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 |
| Bora Pharmaceutical Laboratories Inc. Zhongli Plant | Taoyuan City, Taiwan | Makes it and tests it | Problems found, fixed voluntarilyFeb 7, 2020 · 4 inspections |
| Formosa Laboratories, Inc. | Taoyuan, Taiwan | Makes the active ingredient | Problems found, fixed voluntarilyJul 25, 2024 · 6 inspections |
| Apace Packaging LLC | Fountain Run, KY, United States | Packages it and labels it | No problems foundJan 13, 2022 · 6 inspections |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
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 30, 2019
- Package NDCs
71205-966-67- Official label
- DailyMed (National Library of Medicine), updated May 1, 2024
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