NDC 70518-4241
Lurasidone hydrochloride 20 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-351.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Srikakulam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 20, 2022 · 5 inspections |
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA208047
- On the market since
- Dec 16, 2024
- Package NDCs
70518-4241-0- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2026
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