FDAFDA · Food and drugs·Recall number D-0135-2025
Levothyroxine Sodium Tablets, USP, 150 mcg (0.150 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: 51079-445-20
Published December 18, 2024 · Recall initiated: November 19, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Subpotent and Superpotent Drug
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- LEVOTHYROXINE SODIUM
- Manufacturer
- Mylan Institutional, Inc.
- Distributor
- Nationwide in the USA.
- Lot
- Lot #: 3115924, Exp. Date 06/2025
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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