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
71610-744_5866cff8-7c35-4050-a75f-5e235b9d39b2
Product NDC
71610-744
Form
TABLET, FILM COATED
Composition / generic term
ATORVASTATIN CALCIUM
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20230810
Source listing expiry
20261231

Source-listed ingredients

  • ATORVASTATIN CALCIUM TRIHYDRATE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 15 TABLET, FILM COATED in 1 BOTTLE (71610-744-15) · 71610-744-15
  • 30 TABLET, FILM COATED in 1 BOTTLE (71610-744-30) · 71610-744-30
  • 45 TABLET, FILM COATED in 1 BOTTLE (71610-744-45) · 71610-744-45
  • 60 TABLET, FILM COATED in 1 BOTTLE (71610-744-53) · 71610-744-53
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-744-60) · 71610-744-60
  • 120 TABLET, FILM COATED in 1 BOTTLE (71610-744-70) · 71610-744-70

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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