NDC 50436-0054

Escitalopram 20 mg tablet, film coated

On the label: Unit Dose Services. It's a repackaged product (source NDC 60505-2782, 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 and relabels 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 Unit Dose Services uses for other drugs.

Product details

Generic drug

Escitalopram: see every company that makes it

Form

tablet, film coated

Strength

20 mg

Approval

ANDA ANDA078777

On the market since

Sep 11, 2012

Package NDCs

50436-0054-1

Official label

DailyMed (National Library of Medicine), updated Nov 7, 2017

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