NDC 45865-787

Escitalopram 10 mg tablet, film coated

On the label: Medsource Pharmaceuticals. It's a repackaged product (source NDC 0093-5851, 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 Medsource Pharmaceuticals uses for other drugs.

Product details

Generic drug

Escitalopram: see every company that makes it

Form

tablet, film coated

Strength

10 mg

Approval

ANDA ANDA076765

On the market since

Mar 14, 2012

Package NDCs

45865-787-30

Official label

DailyMed (National Library of Medicine), updated Dec 20, 2018

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