Thyroid Tablets
Superpotent Drug
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Subpotent and Superpotent Drug
Cause type: Wrong potency / content
Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.
Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 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: 51079-442-20
Compare with the code on your package — it is the most precise check available.
Drug: Levothyroxine Category: Thyroid Medication
From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.
| Product | Strength | Form & route | Labeler | Type |
|---|---|---|---|---|
| Levothyroxine Sodium NDC 51079-0442 |
100 ug/1 | Tablet Oral |
Mylan Institutional Inc. | Rx |
Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.
Superpotent Drug
Subpotent Drug
Subpotent Drug
Subpotent Drug
Subpotent Drug
Super-Potent Drug: Out of specification potency results were obtained.
Super-Potent Drug: Out of specification potency results were obtained.
Subpotent and Superpotent Drug
Subpotent and Superpotent Drug
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