Viatris Inc recalls Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV
Recalled May 8, 2024 · FDA recall D-0481-2024 · Viatris
Hazard
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets. · FDA Class III
Units
143,230 bottles
Sold at
Nationwide within the united states
Description
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
Product
Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77
Manufacturer(s)
Viatris Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →