NDC 0406-1180
Quetiapine FumarateExtended-Release 50 mg tablet, extended release
On the label: SpecGx LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| IntelliPharmaCeutics Corp. | Location not on file | Makes it and packages it | Not inspected on record |
| Zhejiang SyncoTide Bio-pharmaceutical Co., Ltd | Shaoxing, China | Makes the active ingredient | Problems found, fixed voluntarilyMar 7, 2025 · 5 inspections |
Product details
- Generic drug
- Quetiapine: every company that makes it
- Form
- tablet, extended release
- Strength
- 50 mg
- Approval
- ANDA ANDA202939
- On the market since
- May 15, 2017
- Package NDCs
0406-1180-60- Official label
- DailyMed (National Library of Medicine), updated Jan 4, 2019
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