Class II ยท Moderate risk
Sotalol HCL
Labeling: Label Mixup: SOTALOL HCL, Tablet, 160 mg may have potentially been mislabeled as the following drug: DISULFIRAM, Tablet, 250 mg, NDC 64980017101, Pedigree: AD22609_1, EXP: 5/2/2014.
National Drug Code
Is NDC 0093-1062-01 recalled?
Sotalol Hydrochloride · 100 TABLET in 1 BOTTLE (0093-1062-01)
Yes — this exact package was recalled
1 FDA recall names the code 0093-1062-01 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
- Sotalol Hydrochloride
- Strength
- SOTALOL HYDROCHLORIDE 160 mg/1
- Form
- Tablet · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-1062
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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