NDC 45865-699

Escitalopram 20 mg tablet, film coated

On the label: Medsource Pharmaceuticals. It's a repackaged product: Medsource Pharmaceuticals rebottles it from Accord Healthcare Inc.'s NDC 16729-170.

Where the pills inside were made

Intas Pharmaceuticals Limited

Ahmedabad, India · makes it and tests it

No problems found Last FDA inspection Jul 12, 2024. 10 inspections on record.

Intas Pharmaceuticals Limited

Ahmedabad, India · makes it and tests it

Serious problems, FDA action Last FDA inspection Dec 2, 2022. 7 inspections on record, 1 with serious problems.

Repackaging site

Product details

Generic drug
Escitalopram: see every company that makes it
Form
tablet, film coated
Strength
20 mg
Approval
ANDA ANDA202389
On the market since
Mar 21, 2013
Package NDCs
45865-699-30
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?