Valacyclovir Tablets USP recall
Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77
Why was Valacyclovir Tablets USP recalled?
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 3183269, Exp. Date May 2025; 3157326, Exp. date June 2024
- Product
- Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77
- Recalling firm
- Viatris Inc
- Quantity
- 143,230 bottles
- Distribution
- Nationwide within the united states
- Recall date
- May 8, 2024
- Classification
- Class III
- Status
- Completed
- Agency
- FDA (drug)