Class II · Moderate risk
Levothyroxine Sodium Tablets
Subpotent Drug
National Drug Code
Is NDC 55154-3559-00 recalled?
Levothyroxine Sodium · 10 BLISTER PACK in 1 BAG (55154-3559-0) / 1 TABLET in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 55154-3559-00 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 .05 mg/1
- Form
- Tablet · Oral
- Labeler
- Cardinal Health 107, LLC
- Type
- Human Prescription Drug
- Product code
- 55154-3559
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
- 55154-3363 Gabapentin 2
- 55154-3543 Enoxaparin Sodium 1
- 55154-3558 Levothyroxine Sodium 1
- 55154-3560 Levothyroxine Sodium 1
- 55154-3562 Levothyroxine Sodium 1
- 55154-3563 Levothyroxine Sodium 1
Free recall alerts
Know the day your medication is recalled
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