Class II · Moderate risk
Levoxyl (levothyroxine sodium)
Subpotent Drug: The products were below specification for potency at the expiry stability point.
National Drug Code
Is NDC 60793-0853-10 recalled?
Levoxyl · 1000 TABLET in 1 BOTTLE (60793-853-10)
Yes — this exact package was recalled
2 FDA recalls name the code 60793-0853-10 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 88 ug/1
- Form
- Tablet · Oral
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Type
- Human Prescription Drug
- Product code
- 60793-0853
Recalls naming this package
Class II · Moderate risk
Levoxyl (levothyroxine sodium)
Chemical contamination: emission of strong odor after package was opened..
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
- 60793-0851 Levoxyl 3
- 60793-0855 Levoxyl 3
- 60793-0858 Levoxyl 3
- 60793-0860 Levoxyl 3
- 60793-0701 Bicillin L-A 2
- 60793-0850 Levoxyl 2
Free recall alerts
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