Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0456-0458-01 recalled?

Armour Thyroid · 100 TABLET in 1 BOTTLE (0456-0458-01)

Yes — this exact package was recalled

1 FDA recall names the code 0456-0458-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Thyroid, Porcine
Strength
SUS SCROFA THYROID 30 mg/1
Form
Tablet · Oral
Labeler
Allergan, Inc.
Type
Human Prescription Drug
Product code
0456-0458

Recalls naming this package

Class II · Moderate risk

Thyroid

Labeling: Label Mixup: THYROID, Tablet, 30 mg may have potentially been mislabeled as one of the following drugs: OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1110 mg, NDC 11523726503, Pedigree: AD70655_20, EXP: 5/29/2014; NICOTINE POLACRILEX, LOZENGE, 2 mg, NDC 37205098769, Pedigree: AD73623_7, EXP: 5/30/2014; PYRIDOXINE HCL, Tablet, 50 mg, NDC 51645090901, Pedigree: W002697, EXP: 6/5/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-913-2014

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler