NDC 54458-937

Lovastatin 20 mg tablet

On the label: International Laboratories, LLC.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Lupin LimitedSalcette, IndiaMakes it Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action

Product details

Generic drug
Lovastatin: every company that makes it
Form
tablet
Strength
20 mg
Approval
ANDA ANDA078296
On the market since
Apr 3, 2010
Package NDCs
54458-937-10 54458-937-16
Official label
DailyMed (National Library of Medicine), updated Oct 31, 2017

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