United States · FDA National Drug Code directory
Simvastatin
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
- 71335-1891_b410c937-f9a1-4089-8ede-265c2dbc32d4
- Product NDC
- 71335-1891
- Form
- TABLET, FILM COATED
- Composition / generic term
- Simvastatin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151217
- Source listing expiry
- 20261231
Source-listed ingredients
- SIMVASTATIN — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1891-1) · 71335-1891-1
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1891-2) · 71335-1891-2
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1891-3) · 71335-1891-3
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1891-4) · 71335-1891-4
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-1891-5) · 71335-1891-5
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-1891-6) · 71335-1891-6
- 3 TABLET, FILM COATED in 1 BOTTLE (71335-1891-7) · 71335-1891-7
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-1891-8) · 71335-1891-8
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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