NDC 60687-758
Lurasidone Hydrochloride 40 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Ascend Laboratories, LLC's NDC 67877-639.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Lurasidone: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA212244
- On the market since
- Jul 3, 2023
- Package NDCs
60687-758-1160687-758-21- Official label
- DailyMed (National Library of Medicine), updated Jan 2, 2025
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