NDC 16571-718
Quetiapine Fumarate 50 mg tablet, film coated
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Quetiapine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA091388
- On the market since
- Mar 27, 2012
- Package NDCs
16571-718-0116571-718-10- Official label
- DailyMed (National Library of Medicine), updated Oct 28, 2025
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