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
- 42385-943_ba8208d7-c3b8-4ddc-8826-9f5265513bfa
- Product NDC
- 42385-943
- Form
- TABLET, FILM COATED
- Composition / generic term
- Atorvastatin Calcium
- Labeler
- Laurus Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240123
- Source listing expiry
- 20261231
Source-listed ingredients
- ATORVASTATIN CALCIUM TRIHYDRATE — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (42385-943-01) · 42385-943-01
- 500 TABLET, FILM COATED in 1 BOTTLE (42385-943-05) · 42385-943-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (42385-943-11) · 42385-943-11
- 30 TABLET, FILM COATED in 1 BOTTLE (42385-943-30) · 42385-943-30
- 8 BLISTER PACK in 1 CARTON (42385-943-64) / 8 TABLET, FILM COATED in 1 BLISTER PACK (42385-943-08) · 42385-943-64
- 10 BLISTER PACK in 1 CARTON (42385-943-68) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42385-943-10) · 42385-943-68
- 90 TABLET, FILM COATED in 1 BOTTLE (42385-943-90) · 42385-943-90
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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