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
- 63629-1018_67bf8a65-3ac2-4e9c-a655-51f0717de716
- Product NDC
- 63629-1018
- 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 (63629-1018-0) · 63629-1018-0
- 100 TABLET in 1 BOTTLE (63629-1018-1) · 63629-1018-1
- 30 TABLET in 1 BOTTLE (63629-1018-2) · 63629-1018-2
- 300 TABLET in 1 BOTTLE (63629-1018-3) · 63629-1018-3
- 120 TABLET in 1 BOTTLE (63629-1018-4) · 63629-1018-4
- 500 TABLET in 1 BOTTLE (63629-1018-5) · 63629-1018-5
- 60 TABLET in 1 BOTTLE (63629-1018-6) · 63629-1018-6
- 800 TABLET in 1 BOTTLE (63629-1018-8) · 63629-1018-8
- 90 TABLET in 1 BOTTLE (63629-1018-9) · 63629-1018-9
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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