Class II · Moderate risk
Levothyroxine Sodium Tablets
Super-Potent Drug: Out of specification potency results were obtained.
National Drug Code
Is NDC 51079-0443-20 recalled?
Levothyroxine Sodium · 100 BLISTER PACK in 1 CARTON (51079-443-20) / 1 TABLET in 1 BLISTER PACK (51079-443-01)
Yes — this exact package was recalled
2 FDA recalls name the code 51079-0443-20 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.
2 of these recalls are still ongoing.
- Active ingredient
- levothyroxine sodium
- Strength
- LEVOTHYROXINE SODIUM 125 ug/1
- Form
- Tablet · Oral
- Labeler
- Mylan Institutional Inc.
- Type
- Human Prescription Drug
- Product code
- 51079-0443
Recalls naming this package
Class II · Moderate risk
Levothyroxine Sodium Tablets
Subpotent and Superpotent Drug
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
- 51079-0445 Levothyroxine Sodium 2
- 51079-0881 See recall 2
- 51079-0947 See recall 2
- 51079-0020 See recall 1
- 51079-0088 Mirtazapine 1
- 51079-0090 See recall 1
Free recall alerts
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