NDC 70518-4491
Lurasidone Hydrochloride 40 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-081.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Annora Pharma Private Limited | Sangareddy, India | Makes it | Problems found, fixed voluntarilyMar 28, 2025 · 4 inspections |
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA218174
- On the market since
- Oct 4, 2025
- Package NDCs
70518-4491-0- Official label
- DailyMed (National Library of Medicine), updated Sep 14, 2026
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