United States · FDA National Drug Code directory
Fluvastatin Sodium
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
- 0093-7446_82469f87-7755-4dda-a92d-a27856d0fe0e
- Product NDC
- 0093-7446
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Fluvastatin Sodium
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160602
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUVASTATIN SODIUM — 80 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-01) · 0093-7446-01
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-56) · 0093-7446-56
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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