Nebivolol Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIIOngoing
Summary: Glenmark Pharmaceuticals Inc., USA is recalling 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.. Reason: Cross Contamination with Other Products.
What is being recalled
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.
Why
Cross Contamination with Other Products
How serious is it
Class III is the least serious level: using or being exposed to this product is not likely to cause health problems, but it breaks FDA rules.
Where it was sold
U.S. Nationwide
How to tell if yours is affected
Lot# 17240988; Exp. 05/31/2026
What to do
Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.
Recall facts
| Recall number | D-0222-2026 |
| Category | Drug |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class III |
| Status | Ongoing |
| Recall started | November 18, 2025 |
| Reported | December 17, 2025 |
| Company | Glenmark Pharmaceuticals Inc., USA |
| Company location | Mahwah, NJ, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 672 90-count bottles |
More recalls from Glenmark Pharmaceuticals Inc., USA · all drug recalls · recalls from November 2025