NDC 43598-351
Lurasidone hydrochloride 20 mg tablet, film coated
On the label: Dr. Reddy's Laboratories Inc..
Where it's 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
- Feb 20, 2023
- Package NDCs
43598-351-0543598-351-3043598-351-7843598-351-7943598-351-90- Official label
- DailyMed (National Library of Medicine), updated Feb 25, 2025
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