Viatris Inc recalls Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only, Distributed by Viatris Specialty LLC, Mo
Recalled January 22, 2025 · FDA recall D-0203-2025 · Viatris
Hazard
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing. · FDA Class II
Units
1,215/30 count bottles
Sold at
USA nationwide.
Description
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.
Product
Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV 26505, NDC 58151-079-93
Manufacturer(s)
Viatris Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →