NDC 70518-4563
Lurasidone Hydrochloride 20 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-080.
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
- 20 mg
- Approval
- ANDA ANDA218174
- On the market since
- Feb 3, 2026
- Package NDCs
70518-4563-0- Official label
- DailyMed (National Library of Medicine), updated Feb 6, 2026
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