NDC 60687-382
Quetiapine fumarate 400 mg tablet
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from BluePoint Laboratories.'s NDC 68001-181.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
| Lupin Limited | Pithampur, India | Makes it | Serious problems, FDA actionJul 17, 2025 · 6 inspections, 4 with FDA action |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Quetiapine: every company that makes it
- Form
- tablet, oral
- Strength
- 400 mg
- Approval
- ANDA ANDA201109
- On the market since
- Oct 3, 2017
- Package NDCs
60687-382-0160687-382-11- Official label
- DailyMed (National Library of Medicine), updated May 21, 2026
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