Alvogen recalls Levothyroxine Sodium Tablets 150mcg over bottle with wrong strength tablets
A pharmacy reported that a single bottle from this lot held 88 mcg tablets instead of 150 mcg tablets because of a product mix-up.
What to do
The notice does not give instructions. Read the official notice for details.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Recall details
- Product
- Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, 1000 Tablets, Rx only, Manufactured by: LLOYD, Inc., Shenandoah, IA, 51601 USA, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC: 47781-662-10.
- Company
- Alvogen, Inc
- Hazard
- Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.
- Where sold
- US Nationwide.
- FDA classification
- Class II · Ongoing
- Classified by FDA
- January 14, 2026
- Recall started
- December 31, 2025
- FDA enforcement report
- January 21, 2026
- Identifiers
- Codes: Lot # MHA21825, Exp Date: December 31, 2027
- FDA recall number: D-0259-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- Product
- Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, 1000 Tablets, Rx only, Manufactured by: LLOYD, Inc., Shenandoah, IA, 51601 USA, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC: 47781-662-10.
- Reason for recall
- Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.
- Classification
- Class II (Ongoing)
- Distribution
- US Nationwide.
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