NDC 67046-1654
Lurasidone Hydrochloride 60 mg tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Aurobindo Pharma Limited's NDC 65862-955.
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
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, oral
- Strength
- 60 mg
- Approval
- ANDA ANDA208045
- On the market since
- Jan 28, 2026
- Package NDCs
67046-1654-3- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2026
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