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

FDA recall notice · announced May 8, 2024 · Viatris

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

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

Reason for recall

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

Notes

Distribution: Nationwide within the united states
Lot/code information: Lot #: 3183269, Exp. Date May 2025; 3157326, Exp. date June 2024
Quantity: 143,230 bottles
Status: Completed
Products in this recall event:
- Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77 (D-0481-2024)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.