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
16714-681_6c353eba-27f3-43cc-b954-ec659881872f
Product NDC
16714-681
Form
TABLET, FILM COATED
Composition / generic term
Simvastatin
Labeler
NorthStar Rx LLC
Marketing category
ANDA
Marketing start / end (source format)
20061220
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 (16714-681-01) · 16714-681-01
  • 90 TABLET, FILM COATED in 1 BOTTLE (16714-681-02) · 16714-681-02

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →