NDC 82804-211
Ezetimibe 10 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-226.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
| Glenmark Pharmaceuticals Limited | Dhar, India | Makes it and tests it | Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Ezetimibe: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA078560
- On the market since
- Apr 29, 2022
- Package NDCs
82804-211-30- Official label
- DailyMed (National Library of Medicine), updated Mar 1, 2025
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