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
71610-250_e41229de-e579-41f7-bfc0-a9fcef4abe0d
Product NDC
71610-250
Form
TABLET, FILM COATED
Composition / generic term
simvastatin
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20080226
Source listing expiry
20261231

Source-listed ingredients

  • SIMVASTATIN — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (71610-250-30) · 71610-250-30
  • 45 TABLET, FILM COATED in 1 BOTTLE (71610-250-45) · 71610-250-45
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-250-60) · 71610-250-60

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 →
simvastatin — United States | Molindra Medicines