NDC 10135-659
QuetiapineExtended Release 400 mg tablet, film coated, extended release
On the label: Marlex Pharmaceuticals, Inc.. It's repackaged: Marlex Pharmaceuticals, Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-384.
Where the pills inside were 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
- Strength
- 400 mg
- Approval
- ANDA ANDA209635
- On the market since
- May 1, 2018
- Package NDCs
10135-659-60- Official label
- DailyMed (National Library of Medicine), updated May 25, 2018
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