NDC 67046-1623
Quetiapine 200 mg tablet, extended release
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from BluePoint Laboratories.'s NDC 68001-600.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unichem Laboratories Limited | Bardez, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 15, 2024 · 6 inspections |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Quetiapine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA215478
- On the market since
- Dec 16, 2025
- Package NDCs
67046-1623-3- Official label
- DailyMed (National Library of Medicine), updated Dec 16, 2025
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