Recall
FDAHealthNovember 18, 2024

Viatris Inc — Levothyroxine Sodium Tablets USP, 50 mcg, packaged in a) 90-count bottles (NDC 0378-1803-77) and b) 1000-count bottles (NDC 0378-1803-10), Rx only, Manufactured for: Mylan Pharmaceutical

⚠️ Superpotent Drug and Subpotent Drug: potency failures obtained

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
November 18, 2024

Nationwide within the United States and Puerto Rico

What's affected?

Product
Levothyroxine Sodium Tablets USP, 50 mcg, packaged in a) 90-count bottles (NDC 0378-1803-77) and b) 1000-count bottles (NDC 0378-1803-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.
Lot code
a)

Additional details

Lot #: a) 8174701, Exp. Date April 2025; 8182228, Exp. Date Aug 2025 b)3193984, Exp. Date Mar 2025; 3206790, Exp. Date Aug 2025

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 42,331 bottles.

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.