NDC 65862-038

Lisinopril 5 mg tablet

On the label: Aurobindo Pharma Limited.

India: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Apl Healthcare LimitedTirupati, IndiaMakes it and tests it Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Lisinopril: every company that makes it
Form
tablet, oral
Strength
5 mg
Approval
ANDA ANDA077622
On the market since
Feb 22, 2006
Package NDCs
65862-038-00 65862-038-01 65862-038-05 65862-038-30 65862-038-99
Official label
DailyMed (National Library of Medicine), updated Jul 21, 2026

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