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
- 70377-001_4d832ba0-8b5c-de5a-246a-a5f30e884bb4
- Product NDC
- 70377-001
- Form
- TABLET, FILM COATED
- Composition / generic term
- Simvastatin
- Labeler
- Biocon Pharma Inc,
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151217
- Source listing expiry
- 20261231
Source-listed ingredients
- SIMVASTATIN — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (70377-001-12) · 70377-001-12
- 45 TABLET, FILM COATED in 1 BOTTLE (70377-001-13) · 70377-001-13
- 90 TABLET, FILM COATED in 1 BOTTLE (70377-001-14) · 70377-001-14
- 1000 TABLET, FILM COATED in 1 BOTTLE (70377-001-15) · 70377-001-15
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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