NDC 50090-3331
Escitalopram 20 mg tablet, film coated
On the label: A-S Medication Solutions. It's repackaged from NDC 0093-5852, made by Teva Pharmaceuticals USA, Inc. (Escitalopram). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants A-S Medication Solutions names for other drugs.
Product details
- Generic drug
- Escitalopram: every company that makes it
- Form
- tablet, film coated
- Strength
- 20 mg
- Approval
- ANDA ANDA076765
- On the market since
- Mar 14, 2012
- Package NDCs
50090-3331-050090-3331-1- Official label
- DailyMed (National Library of Medicine), updated Mar 1, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?