United States · FDA National Drug Code directory

Lovastatin

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
71610-775_2db77596-4171-4597-ba55-045b97d142ca
Product NDC
71610-775
Form
TABLET
Composition / generic term
Lovastatin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20021125
Source listing expiry
20261231

Source-listed ingredients

  • LOVASTATIN — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE, PLASTIC (71610-775-30) · 71610-775-30
  • 45 TABLET in 1 BOTTLE, PLASTIC (71610-775-45) · 71610-775-45
  • 60 TABLET in 1 BOTTLE, PLASTIC (71610-775-53) · 71610-775-53
  • 90 TABLET in 1 BOTTLE, PLASTIC (71610-775-60) · 71610-775-60
  • 180 TABLET in 1 BOTTLE, PLASTIC (71610-775-80) · 71610-775-80

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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