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
71205-246_8515db73-8e51-4ff6-b0ae-925490fb815d
Product NDC
71205-246
Form
TABLET, FILM COATED
Composition / generic term
ATORVASTATIN CALCIUM
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20180802
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 (71205-246-30) · 71205-246-30
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-246-60) · 71205-246-60
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-246-90) · 71205-246-90

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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