Recall
FDAHealthDecember 23, 2024

Viatris Inc — Cardura XL (doxazosin) extended release tablets 4 mg, 30 -count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV 26505, NDC 58151-078-93

⚠️ Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
December 23, 2024

USA nationwide.

What's affected?

Product
Cardura XL (doxazosin) extended release tablets 4 mg, 30 -count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV 26505, NDC 58151-078-93
Brand
CARDURA
UPC
0358151078936
Lot code
8182298

Additional details

Lot# 8182298, Exp 10/31/2025

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 6,605/30 count bottles.

View original FDA notice →

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