Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77
Reported: May 8, 2024 Initiated: April 25, 2024 #D-0481-2024
Product Description
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.
Details
- Recalling Firm
- Viatris Inc
- Units Affected
- 143,230 bottles
- Distribution
- Nationwide within the united states
- Location
- Canonsburg, PA
Frequently Asked Questions
What product was recalled? ▼
Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-4275-77. Recalled by Viatris Inc. Units affected: 143,230 bottles.
Why was this product recalled? ▼
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 8, 2024. Severity: Low. Recall number: D-0481-2024.
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