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
68788-8625_0f633003-ea4c-45fe-bfd8-9838e31ebb8b
Product NDC
68788-8625
Form
TABLET, FILM COATED
Composition / generic term
atorvastatin calcium
Labeler
Preferred Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240409
Source listing expiry
20271231

Source-listed ingredients

  • ATORVASTATIN CALCIUM TRIHYDRATE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-8625-1) · 68788-8625-1
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-8625-3) · 68788-8625-3
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-8625-6) · 68788-8625-6
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-8625-9) · 68788-8625-9

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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