NDC 50228-382
Quetiapine Extended Release 200 mg tablet, film coated, extended release
On the label: ScieGen Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Quetiapine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA209635
- On the market since
- Nov 29, 2017
- Package NDCs
50228-382-1050228-382-3050228-382-60- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2025
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