NDC 16571-769
Escitalopram Oxalate 5 mg per 5 mL solution
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
- Escitalopram: every company that makes it
- Form
- solution, oral
- Strength
- 5 mg per 5 mL
- Approval
- ANDA ANDA079062
- On the market since
- Apr 3, 2012
- Package NDCs
16571-769-24- Official label
- DailyMed (National Library of Medicine), updated May 25, 2026
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