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
- 16571-137_b94c6347-161c-44f2-8937-34c5098bf755
- Product NDC
- 16571-137
- Form
- TABLET
- Composition / generic term
- atorvastatin calcium, film coated
- Labeler
- Rising Pharma Holdings, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231020
- Source listing expiry
- 20261231
Source-listed ingredients
- ATORVASTATIN CALCIUM TRIHYDRATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE (16571-137-09) · 16571-137-09
- 1000 TABLET in 1 BOTTLE (16571-137-10) · 16571-137-10
- 500 TABLET in 1 BOTTLE (16571-137-50) · 16571-137-50
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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