NDC 33342-423
lurasidone hydrochloride 120 mg tablet, film coated
On the label: Macleods Pharmaceuticals Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Macleods Pharmaceuticals Limited | District Solan, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action |
| Oxalis Labs | Solan, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 2, 2023 · 2 inspections |
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 120 mg
- Approval
- ANDA ANDA212124
- On the market since
- Jun 9, 2023
- Package NDCs
33342-423-0733342-423-10- Official label
- DailyMed (National Library of Medicine), updated Apr 28, 2026
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