NDC 70518-4289

Losartan potassium 100 mg tablet, film coated

On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Macleods Pharmaceuticals Limited's NDC 33342-046.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Macleods Pharmaceuticals LimitedDistrict Solan, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 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
Losartan: every company that makes it
Form
tablet, film coated, oral
Strength
100 mg
Approval
ANDA ANDA202230
On the market since
Feb 14, 2025
Package NDCs
70518-4289-0
Official label
DailyMed (National Library of Medicine), updated Sep 3, 2026

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