NDC 51655-151

Escitalopram 20 mg tablet, film coated

On the label: Northwind Pharmaceuticals. It's a repackaged product (source NDC 0093-5852, which isn't on a current label).

Where it's made

This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 Northwind Pharmaceuticals uses for other drugs.

Product details

Generic drug

Escitalopram: see every company that makes it

Form

tablet, film coated

Strength

20 mg

Approval

ANDA ANDA076765

On the market since

Mar 21, 2014

Package NDCs

51655-151-52

Official label

DailyMed (National Library of Medicine), updated Jun 6, 2014

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?