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
- 65862-052_854ac8f7-cca5-434c-a611-9c1752260d4a
- Product NDC
- 65862-052
- Form
- TABLET, FILM COATED
- Composition / generic term
- Simvastatin
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20061220
- Source listing expiry
- 20271231
Source-listed ingredients
- SIMVASTATIN — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (65862-052-00) · 65862-052-00
- 100 TABLET, FILM COATED in 1 BOTTLE (65862-052-01) · 65862-052-01
- 2500 TABLET, FILM COATED in 1 BOTTLE (65862-052-26) · 65862-052-26
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-052-30) · 65862-052-30
- 45 TABLET, FILM COATED in 1 BOTTLE (65862-052-45) · 65862-052-45
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-052-90) · 65862-052-90
- 1000 TABLET, FILM COATED in 1 BOTTLE (65862-052-99) · 65862-052-99
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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