NDC 82804-215
Lurasidone Hydrochloride 20 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Aurobindo Pharma Limited's NDC 65862-953.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA208045
- On the market since
- Mar 10, 2023
- Package NDCs
82804-215-30- Official label
- DailyMed (National Library of Medicine), updated Apr 1, 2025
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