NDC 70518-4427
lurasidone hydrochloride 40 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-671.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Nagpur, India | Makes it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA208031
- On the market since
- Aug 6, 2025
- Package NDCs
70518-4427-0- Official label
- DailyMed (National Library of Medicine), updated Sep 10, 2026
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