NDC 68071-5248
Escitalopram 20 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-282.
Where the pills inside were made
This label doesn't name the factory that makes the drug. 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 Solco Healthcare U.S., LLC names for other drugs.
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Escitalopram: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA078032
- On the market since
- Mar 15, 2012
- Package NDCs
68071-5248-368071-5248-9- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?