Recall
FDAHealthNovember 18, 2024

Viatris Inc — Levothyroxine Sodium Tablets USP, 150 mcg, packaged in a) 90-count bottles (NDC 0378-1815-77) and b) 1000-count bottles (NDC 0378-1815-10), Rx only, Manufactured for: Mylan Pharmaceutica

⚠️ 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, 150 mcg, packaged in a) 90-count bottles (NDC 0378-1815-77) and b) 1000-count bottles (NDC 0378-1815-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.
Lot code
a)

Additional details

Lot #: a) 8177720, Exp. Date Jun 2025; b) 3200218, Exp. Date Jun 2025

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 9,828 bottles.

View original FDA notice →

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