Class II · Moderate risk
Bystolic (nebivolol)
Failed Dissolution Specification; at the 6-month stability time point
National Drug Code
Is NDC 0456-1420-07 recalled?
Bystolic
Yes — this exact package was recalled
2 FDA recalls name the code 0456-1420-07 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
- nebivolol hydrochloride
- Strength
- NEBIVOLOL HYDROCHLORIDE 20 mg/1
- Form
- Tablet · Oral
- Labeler
- Allergan, Inc.
- Type
- Human Prescription Drug
- Product code
- 0456-1420
Recalls naming this package
Class II · Moderate risk
Bystolic (nebivolol)
Failed Dissolution Specifications: Drug failed stage III dissolution testing.
Class II · Moderate risk
Bystolic (nebivolol)
Failed Dissolution Specifications: One lot of product is being voluntarily recalled because dissolution test results failed to meet specification throughout the product's shelf life.
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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