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

Is NDC 0074-7070-90 recalled?

Synthroid · 90 TABLET in 1 BOTTLE (0074-7070-90)

Yes — this exact package was recalled

1 FDA recall names the code 0074-7070-90 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
Levothyroxine Sodium
Strength
LEVOTHYROXINE SODIUM 175 ug/1
Form
Tablet · Oral
Labeler
AbbVie Inc.
Type
Human Prescription Drug
Product code
0074-7070

Recalls naming this package

Class II ยท Moderate risk

Levothyroxine Sodium

Labeling: Label Mixup: LEVOTHYROXINE SODIUM, Tablet, 175 mcg may have potentially been mislabeled as the following drug: CINACALCET HCL, Tablet, 60 mg, NDC 55513007430, Pedigree: W003742, EXP: 6/26/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-811-2014

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