NDC 71205-993

Lovastatin 20 mg tablet

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Carlsbad Technology, Inc.'s NDC 61442-142.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Carlsbad Technology, Inc.Carlsbad, CA, United StatesMakes it Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections

Repackaging site

Product details

Generic drug
Lovastatin: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA075991
On the market since
Nov 25, 2002
Package NDCs
71205-993-00 71205-993-11 71205-993-30 71205-993-55 71205-993-60 71205-993-90
Official label
DailyMed (National Library of Medicine), updated Jul 1, 2022

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