NDC 31722-080
Lurasidone Hydrochloride 20 mg tablet, film coated
On the label: Camber Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Annora Pharma Private Limited | Sangareddy, India | Makes it | Problems found, fixed voluntarilyMar 28, 2025 · 4 inspections |
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA218174
- On the market since
- Aug 21, 2024
- Package NDCs
31722-080-0531722-080-3031722-080-90- Official label
- DailyMed (National Library of Medicine), updated Jul 19, 2025
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