United States · FDA National Drug Code directory
Fluvastatin
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
- 0093-7442_1fb50b66-e9d0-4fd1-928e-b37c4fff4ccc
- Product NDC
- 0093-7442
- Form
- CAPSULE
- Composition / generic term
- Fluvastatin
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120705
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUVASTATIN SODIUM — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (0093-7442-01) · 0093-7442-01
- 30 CAPSULE in 1 BOTTLE (0093-7442-56) · 0093-7442-56
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 →