Viatris Inc recalls Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only,
See all recalls from Viatris Inc →Recalled Product
Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77
Hazard / Issue
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 3183269, Exp. Date May 2025; 3157326, Exp. date June 2024
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Valacyclovir Tablets USP, 500 →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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