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
- 71335-2591_11e721da-80b6-4730-ad52-ad11ec164696
- Product NDC
- 71335-2591
- Form
- TABLET
- Composition / generic term
- atorvastatin calcium, film coated
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231020
- Source listing expiry
- 20261231
Source-listed ingredients
- ATORVASTATIN CALCIUM TRIHYDRATE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-2591-1) · 71335-2591-1
- 100 TABLET in 1 BOTTLE (71335-2591-2) · 71335-2591-2
- 90 TABLET in 1 BOTTLE (71335-2591-3) · 71335-2591-3
- 60 TABLET in 1 BOTTLE (71335-2591-4) · 71335-2591-4
- 180 TABLET in 1 BOTTLE (71335-2591-5) · 71335-2591-5
- 10 TABLET in 1 BOTTLE (71335-2591-6) · 71335-2591-6
- 7 TABLET in 1 BOTTLE (71335-2591-7) · 71335-2591-7
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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