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Viatris Inc — Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only
Do not stop taking this without speaking to your pharmacist or doctor.
What’s wrong
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
The Recall Registry rates this labelling issue — FDA Class III: unlikely to cause harm.
What to do
Check the lot numbers below against what you have. Do not stop taking a prescription medicine because of a recall without speaking to your pharmacist or doctor first — for many medicines stopping is more harmful than continuing, and they can tell you whether yours is affected and what to do about it.
Who to contact: Recalling firm: Viatris Inc
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
Details
- Units affected
- 143,230 bottles
- Recall date
- April 25, 2024
- Brand
- Viatris Inc
Nationwide within the united states
The official notice
This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.
Their exact wording: “Viatris Inc — Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77”
Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.
Filed under: Prescription medicine