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
- 72162-1739_c3daa4ef-b136-479f-b7f7-48ef98c763d5
- Product NDC
- 72162-1739
- Form
- TABLET
- Composition / generic term
- Lovastatin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20021125
- Source listing expiry
- 20261231
Source-listed ingredients
- LOVASTATIN — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (72162-1739-0) · 72162-1739-0
- 100 TABLET in 1 BOTTLE (72162-1739-2) · 72162-1739-2
- 300 TABLET in 1 BOTTLE (72162-1739-4) · 72162-1739-4
- 500 TABLET in 1 BOTTLE (72162-1739-5) · 72162-1739-5
- 60 TABLET in 1 BOTTLE (72162-1739-6) · 72162-1739-6
- 120 TABLET in 1 BOTTLE (72162-1739-7) · 72162-1739-7
- 90 TABLET in 1 BOTTLE (72162-1739-9) · 72162-1739-9
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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