NDC 42708-155
Escitalopram 10 mg tablet, film coated
On the label: QPharma, Inc..
It's a repackaged product: QPharma, Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-281.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Solco Healthcare U.S., LLC uses for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Escitalopram: see every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA078032
- On the market since
- Feb 1, 2016
- Package NDCs
42708-155-30- Official label
- DailyMed (National Library of Medicine), updated Dec 1, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?