Class II · Moderate risk
Levothyroxine Sodium Tablets
Subpotent and Superpotent Drug
National Drug Code
Is NDC 42292-0039-20 recalled?
Levothyroxine Sodium · 100 BLISTER PACK in 1 CARTON (42292-039-20) / 1 TABLET in 1 BLISTER PACK (42292-039-01)
Yes — this exact package was recalled
1 FDA recall names the code 42292-0039-20 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.
1 of these recalls is still ongoing.
- Active ingredient
- levothyroxine sodium
- Strength
- LEVOTHYROXINE SODIUM 112 ug/1
- Form
- Tablet · Oral
- Labeler
- Mylan Institutional Inc.
- Type
- Human Prescription Drug
- Product code
- 42292-0039
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
- 42292-0009 See recall 1
- 42292-0010 See recall 1
- 42292-0040 Levothyroxine Sodium 1
- 42292-0041 Levothyroxine Sodium 1
Free recall alerts
Know the day your medication is recalled
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