Class II ยท Moderate risk
Synthroid (Levothyroxine Sodium)
Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.
National Drug Code
Is NDC 0074-7069-90 recalled?
Synthroid · 90 TABLET in 1 BOTTLE (0074-7069-90)
Yes — this exact package was recalled
1 FDA recall names the code 0074-7069-90 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 150 ug/1
- Form
- Tablet · Oral
- Labeler
- AbbVie Inc.
- Type
- Human Prescription Drug
- Product code
- 0074-7069
Recalls naming this package
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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