WhichRecall
Class IIReported 2024-12-18

Levothyroxine Sodium Tablets USP, 75 mcg, packaged in a) 90-count bottles (NDC 0378-1805-77) and b) 1000-count bottles (NDC 0378-1805-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.

Recalled by Viatris Inc

Reason for Recall

Superpotent Drug and Subpotent Drug: potency failures obtained

Advertisement
Recall Number
D-0125-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2024-11-18
Reported
2024-12-18
Distribution
Nationwide within the United States and Puerto Rico
Code Info
Lot #: a) 8177078, Exp. Date May 2025; 8168596, Exp. Date Jan 2025 b) 3199313, Exp. Date May 2025; 3194118, Exp. Date Mar 2025; 3186238, Exp. Date Dec 2024; 3209590, Exp. Date Sep 2025; 3199317, Exp. Date May 2025; 3188733, Exp. Date Jan 2025
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
Advertisement