Class III

Drug Recall: Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77

Viatris Inc · April 25, 2024

Reason for Recall

Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.

Distribution

Nationwide within the united states

States Affected

NATIONWIDE

Quantity Affected

143,230 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0481-2024

Status: completed

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.