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
- 55111-122_36e09eff-3948-2638-b633-d5ec2bc03d2a
- Product NDC
- 55111-122
- Form
- TABLET
- Composition / generic term
- Atorvastatin Calcium
- Labeler
- Dr. Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120717
- Source listing expiry
- 20261231
Source-listed ingredients
- ATORVASTATIN CALCIUM TRIHYDRATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (55111-122-05) · 55111-122-05
- 1000 TABLET in 1 BOTTLE (55111-122-10) · 55111-122-10
- 30 TABLET in 1 BOTTLE (55111-122-30) · 55111-122-30
- 60 TABLET in 1 BOTTLE (55111-122-60) · 55111-122-60
- 90 TABLET in 1 BOTTLE (55111-122-90) · 55111-122-90
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 →