NDC 70518-4260
lurasidone hydrochloride 20 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-638.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA212244
- On the market since
- Jan 22, 2025
- Package NDCs
70518-4260-0- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2026
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