NDC 68001-315

Lovastatin 20 mg tablet

On the label: BluePoint Laboratories..

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, oral
Strength
20 mg
Approval
ANDA ANDA078296
On the market since
Nov 1, 2007
Package NDCs
68001-315-00 68001-315-08
Official label
DailyMed (National Library of Medicine), updated Oct 7, 2026

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