NDC 65862-375

Escitalopram 20 mg tablet, film coated

On the label: Aurobindo Pharma Limited.

Where it's made

Aurobindo Pharma Limited

Medchal, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Jul 21, 2023. 13 inspections on record, 1 with serious problems.

Product details

Generic drug

Escitalopram: see every company that makes it

Form

tablet, film coated, oral

Strength

20 mg

Approval

ANDA ANDA090432

On the market since

Sep 11, 2012

Package NDCs

65862-375-01 65862-375-05 65862-375-10 65862-375-30 65862-375-39 65862-375-90

Official label

DailyMed (National Library of Medicine), updated May 12, 2026

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