Class III ยท Low risk
Nebivolol Tablets
Cross Contamination with Other Products
National Drug Code
Is NDC 42291-0874-90 recalled?
nebivolol · 90 TABLET in 1 BOTTLE (42291-874-90)
Yes — this exact package was recalled
1 FDA recall names the code 42291-0874-90 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.
1 of these recalls is still ongoing.
- Active ingredient
- nebivolol hydrochloride
- Strength
- NEBIVOLOL HYDROCHLORIDE 20 mg/1
- Form
- Tablet · Oral
- Labeler
- AvKARE
- Type
- Human Prescription Drug
- Product code
- 42291-0874
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
- 42291-0297 See recall 1
- 42291-0367 Lamotrigine 1
- 42291-0368 Lamotrigine 1
- 42291-0459 See recall 1
- 42291-0460 See recall 1
- 42291-0461 See recall 1
Free recall alerts
Know the day your medication is recalled
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