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
- 75834-256_4580fe3c-b524-3a14-e063-6294a90a34d3
- Product NDC
- 75834-256
- Form
- TABLET
- Composition / generic term
- Atorvastatin calcium
- Labeler
- NIVAGEN PHARMACEUTICALS, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200826
- Source listing expiry
- 20261231
Source-listed ingredients
- ATORVASTATIN — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (75834-256-01) · 75834-256-01
- 5000 TABLET in 1 BOTTLE (75834-256-05) · 75834-256-05
- 500 TABLET in 1 BOTTLE (75834-256-50) · 75834-256-50
- 90 TABLET in 1 BOTTLE (75834-256-90) · 75834-256-90
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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