Viatris Inc recalls Carvedilol Tablets, USP, 25 mg, 500-count bottles, Rx Only, Mfg: Mylan Pharmaceuticals Inc. Morgantown, WV 36505, Made i
Recalled November 23, 2022 · FDA recall D-0063-2023 · Viatris
Hazard
Failed Tablet/Capsule Specifications: Tablets exceeds specification for weight and thickness. · FDA Class II
Units
2,794 bottles
Sold at
Nationwide in the USA
Description
Failed Tablet/Capsule Specifications: Tablets exceeds specification for weight and thickness.
Product
Carvedilol Tablets, USP, 25 mg, 500-count bottles, Rx Only, Mfg: Mylan Pharmaceuticals Inc. Morgantown, WV 36505, Made in India, NDC 0378-3634-05
Manufacturer(s)
Viatris Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →