NDC 68382-965
Lurasidone hydrochloride 20 mg tablet, coated
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections |
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA208052
- On the market since
- Feb 1, 2023
- Package NDCs
68382-965-0168382-965-0568382-965-0668382-965-1668382-965-3068382-965-77- Official label
- DailyMed (National Library of Medicine), updated Jul 28, 2026
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