Class II · Moderate risk
Verapamil HCL ER
Labeling: Label Mixup: VERAPAMIL HCL ER, Capsule, 240 mg may have potentially been mislabeled as the following drug: FEBUXOSTAT, Tablet, 40 mg, NDC 64764091830, Pedigree: W002664, EXP: 6/5/2014.
National Drug Code
Is NDC 0378-6440-01 recalled?
Verapamil Hydrochloride · 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6440-01)
Yes — this exact package was recalled
1 FDA recall names the code 0378-6440-01 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
- verapamil hydrochloride
- Strength
- VERAPAMIL HYDROCHLORIDE 240 mg/1
- Form
- Capsule, Extended Release · Oral
- Labeler
- Mylan Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 0378-6440
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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