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
71335-2977_dc22d1df-cdbf-4bf5-a90a-7c0f2370e030
Product NDC
71335-2977
Form
TABLET, FILM COATED
Composition / generic term
Atorvastatin calcium
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20190208
Source listing expiry
20261231

Source-listed ingredients

  • ATORVASTATIN CALCIUM TRIHYDRATE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-2977-1) · 71335-2977-1
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-2977-2) · 71335-2977-2
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-2977-3) · 71335-2977-3
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-2977-4) · 71335-2977-4
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-2977-5) · 71335-2977-5
  • 180 TABLET, FILM COATED in 1 BOTTLE (71335-2977-6) · 71335-2977-6

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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