United States · FDA National Drug Code directory

Atorvastatin Calcium

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
71335-9723_6b6c1e31-f207-400f-9599-a2f96c5bb3c7
Product NDC
71335-9723
Form
TABLET
Composition / generic term
Atorvastatin Calcium
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20220829
Source listing expiry
20261231

Source-listed ingredients

  • ATORVASTATIN CALCIUM TRIHYDRATE — 40 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (71335-9723-1) · 71335-9723-1
  • 100 TABLET in 1 BOTTLE (71335-9723-2) · 71335-9723-2
  • 90 TABLET in 1 BOTTLE (71335-9723-3) · 71335-9723-3
  • 60 TABLET in 1 BOTTLE (71335-9723-4) · 71335-9723-4
  • 180 TABLET in 1 BOTTLE (71335-9723-5) · 71335-9723-5
  • 10 TABLET in 1 BOTTLE (71335-9723-6) · 71335-9723-6
  • 7 TABLET in 1 BOTTLE (71335-9723-7) · 71335-9723-7

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 →