NDC 65862-373

Escitalopram 5 mg tablet, film coated

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action

Product details

Generic drug
Escitalopram: every company that makes it
Form
tablet, film coated, oral
Strength
5 mg
Approval
ANDA ANDA090432
On the market since
Sep 11, 2012
Package NDCs
65862-373-01 65862-373-05 65862-373-10 65862-373-19 65862-373-30 65862-373-90
Official label
DailyMed (National Library of Medicine), updated May 12, 2026

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