Major Pharmaceuticals Levothyroxine 75mcg Recall
Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed b
Updated July 13, 2026
Major Pharmaceuticals' Levothyroxine Sodium Tablets, USP 75 mcg, have been found to be subpotent, meaning they contain less active ingredient than stated. Patients taking this medication may not receive the full therapeutic dose needed to manage their thyroid condition.
Is the Major Pharmaceuticals recalled? Yes. This product was recalled by FDA on July 13, 2026. Details below.
What is recalled
Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), packaged in 10 x 1 unit dose blisters per carton, Rx only. Packaged and distributed by Major Pharmaceuticals, Indianapolis, IN 46268. Distributed by Cardinal Health, Dublin, OH 43017. NDC Bag: 55154-3560-0; NDC Blister: 0904-6951-61.
Am I affected
You're affected if you have a prescription for Levothyroxine Sodium Tablets 75 mcg in unit dose blisters from Major Pharmaceuticals with NDC Bag 55154-3560-0 or NDC Blister 0904-6951-61. Check the label on your medication bottle or blister pack for these numbers.
What to do right now
Stop taking this medication and contact your pharmacist or doctor right away. Do not discontinue thyroid treatment on your own; your healthcare provider will advise you on what to do next, which may include a replacement supply or dosage adjustment.
The hazard
Subpotent Drug
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0709-2026
- Classification
- Class II
- Recalled
- July 13, 2026
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