US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 6, 2023 (4 years ago)

Levothyroxine Sodium Tablets, USP 112 mcg, 90 tablets per bottle, Rx Only, Manufactured…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Sub-Potent Drug: Out of specification for assay at the 24 month interval.

What was recalled

Levothyroxine Sodium Tablets, USP 112 mcg, 90 tablets per bottle, Rx Only, Manufactured by Lloyd Inc., Shenandoah, IA, 51601, Distributed by: Alvogen Inc, Pine Brook, NJ 07058, NDC 47781-654-90.

Recalling firm
Alvogen, Inc
NDC code
47781-654-90
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0353-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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