Aurobindo Pharma Limited
Medchal, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Jul 21, 2023. 13 inspections on record, 1 with serious problems.
NDC 68084-618
Escitalopram 20 mg tablet, film coated
On the label: American Health Packaging.
It's a repackaged product: American Health Packaging rebottles it from Aurobindo Pharma Limited's NDC 65862-375.
Where the pills inside were made
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Escitalopram: see every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA090432
- On the market since
- Oct 8, 2012
- Package NDCs
68084-618-0168084-618-11- Official label
- DailyMed (National Library of Medicine), updated Mar 21, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?