Recalling firm
Viatris Inc
Product type
Drug
Status
Completed
Report date
2024-05-08
Distribution
Nationwide within the united states
Firm state
PA
Product quantity
143,230 bottles
Initiated by
Voluntary: Firm initiated
Reason for recall
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
Product description
Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77
Code / lot info
Lot #: 3183269, Exp. Date May 2025; 3157326, Exp. date June 2024
Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.