NDC 65862-248

Escitalopram Oxalate 5 mg per 5 mL solution

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
solution, oral
Strength
5 mg per 5 mL
Approval
ANDA ANDA079062
On the market since
Apr 3, 2012
Package NDCs
65862-248-24
Official label
DailyMed (National Library of Medicine), updated Oct 12, 2026

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