Class III · Lower riskActive recall
Nebivolol
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot# 17240988; Exp. 05/31/2026
Where it was soldU.S. Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Cross Contamination with Other Products
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made byGlenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for Avkare, Pulaski, TN 38478, Product of Italy foreign manufacturer
| Brand name | NEBIVOLOL |
| Generic name | NEBIVOLOL HYDROCHLORIDE |
| Active ingredient(s) | NEBIVOLOL HYDROCHLORIDE |
| Distributed by / for | Avkare, Pulaski, TN 38478, Product of Italy |
| NDC | 42291-874-90 |
Show the full FDA record
| Full product label | Nebivolol Tablets, 20 mg, 90 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for Avkare, Pulaski, TN 38478, Product of Italy, NDC 42291-874-90. |
| Recalling firm | Glenmark Pharmaceuticals Inc., USA |
| Distribution | U.S. Nationwide |
| Quantity | 672 90-count bottles |
| Recall initiated | 2025-11-18 |
| Report date | 2025-12-17 |
| Recall completed | — |
| Recall number | D-0222-2026 |
| Classification | Class III |
| FDA status | Ongoing |
| Origin on file | Mahwah NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.