TheraRadar
Data updated: May 26, 2026

FLUVASTATIN SODIUM

Cardiovascular Approved 2012-04-11

Fluvastatin sodium is indicated as an adjunct to diet to reduce low-density lipoprotein cholesterol (LDL-C) in adults with primary hyperlipidemia and in adults and pediatric patients (aged 10 and older) with heterozygous familial hypercholesterolemia. In patients with clinically evident coronary heart disease, it is used to slow the progression of coronary atherosclerosis and reduce the risk of undergoing coronary revascularization procedures.

Source: FDA Label • Teva

How FLUVASTATIN SODIUM Works

Fluvastatin is a competitive inhibitor of HMG-CoA reductase, the rate-limiting enzyme that converts HMG-CoA to mevalonate, a precursor of cholesterol. By inhibiting this pathway, it reduces endogenous cholesterol synthesis.

Source: FDA Label
5
Indications
--
Phase 3 Trials
14
Years on Market

Details

Status
Prescription
First Approved
2012-04-11
Routes
ORAL
Dosage Forms
TABLET, EXTENDED RELEASE, CAPSULE

FLUVASTATIN SODIUM Approval History

2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
25 FDA actions from 2012 to 2024
Sep 2024 SUPPL
Label · Labeling
Jul 2024 SUPPL
Label · Labeling
Jul 2023 SUPPL
Label · Labeling

What FLUVASTATIN SODIUM Treats

4 indications

FLUVASTATIN SODIUM is approved for 4 conditions since its original approval in 2012. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Coronary Heart Disease
  • Coronary Atherosclerosis
  • Primary Hyperlipidemia
  • Heterozygous Familial Hypercholesterolemia
Source: FDA Label

FLUVASTATIN SODIUM Competitive Set

Pro

Three rings of competition based on shared molecular targets and treated indications.

Unlock 16 more competitors across all three rings.
Upgrade to Pro

Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

Drugs Similar to FLUVASTATIN SODIUM

3 of 19

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

ATORVALIQ
ATORVASTATIN CALCIUM
3 shared
CMP DEV LLC
Shared indications:
Coronary Heart DiseasePrimary HyperlipidemiaHeterozygous Familial Hypercholesterolemia
FLOLIPID
SIMVASTATIN
3 shared
SALERNO PHARMS
Shared indications:
Coronary Heart DiseasePrimary HyperlipidemiaHeterozygous Familial Hypercholesterolemia
LESCOL XL
FLUVASTATIN SODIUM
3 shared
Novartis
Shared indications:
Coronary Heart DiseaseCoronary AtherosclerosisHeterozygous Familial Hypercholesterolemia
📋

Clinical Trial Registry

1 trials
Trial Sponsor ID Phase Status Title
NCT01551173 results posted CXUO320BCN01 Ph 4 completed Efficacy and Safety of Fluvastatin Sodium Extended Release Tablets 80 mg Once Daily in Chinese Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia
🔬

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
📊

Trial Timeline

Full development history with FDA approval milestones

|
Loading...
Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

FLUVASTATIN SODIUM FDA Label Details

Indications & Usage

FLUVASTATIN SODIUM is indicated for the treatment of Coronary Heart Disease; Coronary Atherosclerosis; Primary Hyperlipidemia; Heterozygous Familial Hypercholesterolemia.

Looking for the branded version?

LESCOL XL

Full clinical data, patents, trials, and competitive landscape for fluvastatin sodium.

See LESCOL XL

Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.