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
71335-3179_4c68ba68-378b-4e23-b8da-9af11d4963a2
Product NDC
71335-3179
Form
TABLET, FILM COATED
Composition / generic term
Atorvastatin Calcium
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20240213
Source listing expiry
20271231

Source-listed ingredients

  • ATORVASTATIN CALCIUM TRIHYDRATE — 80 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-3179-1) · 71335-3179-1
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-3179-2) · 71335-3179-2
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-3179-3) · 71335-3179-3
  • 180 TABLET, FILM COATED in 1 BOTTLE (71335-3179-4) · 71335-3179-4

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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