Class II · Moderate risk
Mexiletine HCL
Labeling: Label Mixup: MEXILETINE HCL, Capsule, 150 mg may have potentially been mislabeled as the following drug: CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD62865_4, EXP: 5/23/2014.
National Drug Code
Is NDC 0093-8739-01 recalled?
Mexiletine Hydrochloride · 100 CAPSULE in 1 BOTTLE (0093-8739-01)
Yes — this exact package was recalled
1 FDA recall names the code 0093-8739-01 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
- Mexiletine Hydrochloride
- Strength
- MEXILETINE HYDROCHLORIDE 150 mg/1
- Form
- Capsule · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-8739
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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