Class III · Low risk
Synthroid
Labeling: Wrong Barcode- One (1) of every forty (40) unit dose blister will contain incorrect barcode information that causes a 125mcg unit dose is scanned as 200mcg unit dose.
National Drug Code
Is NDC 0074-7068-11 recalled?
Synthroid · 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-7068-11) / 10 TABLET in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 0074-7068-11 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.
1 of these recalls is still ongoing.
- Active ingredient
- Levothyroxine Sodium
- Strength
- LEVOTHYROXINE SODIUM 125 ug/1
- Form
- Tablet · Oral
- Labeler
- AbbVie Inc.
- Type
- Human Prescription Drug
- Product code
- 0074-7068
Recalls naming this package
Class II · Moderate risk
Levothyroxine Sodium
Labeling: Label Mixup: LEVOTHYROXINE SODIUM, Tablet, 125 mcg may have potentially been mislabeled as the following drug: MAGNESIUM CHLORIDE DR, Tablet, 64 mg, NDC 00904791152, Pedigree: AD70615_1, EXP: 2/28/2014.
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
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