NDC 42708-077
Escitalopram 10 mg tablet, film coated
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-374.
Where the pills inside were 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 |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Escitalopram: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA090432
- On the market since
- Sep 11, 2012
- Package NDCs
42708-077-30- Official label
- DailyMed (National Library of Medicine), updated Dec 1, 2025
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