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: 71205-440_027bd594-6a0a-4e6d-bd3c-4f33fdb4166a
Product NDC: 71205-440
Form: TABLET
Composition / generic term: Lovastatin
Labeler: Proficient Rx LP
Marketing category: ANDA
Marketing start / end (source format): 20011217
Source listing expiry: 20261231

Source-listed ingredients

LOVASTATIN — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE (71205-440-30) · 71205-440-30
60 TABLET in 1 BOTTLE (71205-440-60) · 71205-440-60
90 TABLET in 1 BOTTLE (71205-440-90) · 71205-440-90

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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