FDAFDA · Food and drugs·Recall number D-0481-2024
Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77
Published May 8, 2024 · Recall initiated: April 25, 2024
Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- VALACYCLOVIR HYDROCHLORIDE
- Manufacturer
- Viatris Inc
- Distributor
- Nationwide within the united states
- UPC
- 0303784276938
- Lot
- Lot #: 3183269, Exp. Date May 2025; 3157326, Exp. date June 2024
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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