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
- 69097-899_ee5777b3-1606-4a9c-b761-211b47d28522
- Product NDC
- 69097-899
- Form
- TABLET, FILM COATED
- Composition / generic term
- ATORVASTATIN CALCIUM
- Labeler
- Cipla USA Inc.,
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160804
- Source listing expiry
- 20261231
Source-listed ingredients
- ATORVASTATIN CALCIUM TRIHYDRATE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, FILM COATED in 1 BOTTLE (69097-899-05) · 69097-899-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (69097-899-15) · 69097-899-15
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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