NDC 64205-585

Escitalopram 10 mg tablet, film coated

On the label: ReadyMeds. 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 ReadyMeds 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
64205-585-30 64205-585-90
Official label
DailyMed (National Library of Medicine), updated May 5, 2014

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