NDC 80425-0375
Escitalopram 10 mg tablet, film coated
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC 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
- Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN, 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
- Mar 13, 2024
- Package NDCs
80425-0375-180425-0375-280425-0375-3- Official label
- DailyMed (National Library of Medicine), updated Mar 19, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?