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
- 0093-5057_53f151e2-6323-4661-ad59-3c433c8ad1d4
- Product NDC
- 0093-5057
- Form
- TABLET, FILM COATED
- Composition / generic term
- Atorvastatin Calcium
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170504 / 20271130
Source-listed ingredients
- ATORVASTATIN CALCIUM TRIHYDRATE — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED in 1 BOTTLE (0093-5057-05) · 0093-5057-05
- 90 TABLET, FILM COATED in 1 BOTTLE (0093-5057-98) · 0093-5057-98
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →