NDC 70518-4173
Lurasidone Hydrochloride 40 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-954.
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 |
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet
- Strength
- 40 mg
- Approval
- ANDA ANDA208045
- On the market since
- Sep 4, 2024
- Package NDCs
70518-4173-0- Official label
- DailyMed (National Library of Medicine), updated Sep 26, 2025
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