TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

CARDURA XL

DOXAZOSIN MESYLATE
Cardiovascular Approved 2005-02-22
1
Indication
--
Phase 3 Trials
21
Years on Market

Details

Status
Prescription
First Approved
2005-02-22
Routes
ORAL
Dosage Forms
TABLET, EXTENDED RELEASE

Companies

Active Ingredient: DOXAZOSIN MESYLATE

CARDURA XL Approval History

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What CARDURA XL Treats

1 indications

CARDURA XL is approved for 1 conditions since its original approval in 2005. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Benign Prostatic Hyperplasia
Source: FDA Label
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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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.

CARDURA XL FDA Label Details

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Indications & Usage

FDA Label (PDF)

CARDURA ® XL is indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH). CARDURA XL is not indicated for the treatment of hypertension. CARDURA XL is an alpha 1 adrenergic antagonist indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia. CARDURA XL is not indicated for the treatment of hypertension.

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Data Sources

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