WhichRecall
Class IIReported 2024-12-18

Levothyroxine Sodium Tablets, USP, 137 mcg (0.137 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-041-20

Recalled by Mylan Institutional, Inc.

Reason for Recall

Subpotent and Superpotent Drug

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Recall Number
D-0134-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2024-11-19
Reported
2024-12-18
Distribution
Nationwide in the USA.
Code Info
Lot #: 3115448, Exp. Date 12/31/2024;3115732, Exp. Date 3/31/2025; 3116024, Exp. Date 9/30/2025
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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