PlainRecalls
FDA Drug Low Class III Ongoing

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.

Reported: December 17, 2025 Initiated: November 18, 2025 #D-0222-2026

Product Description

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 for Recall

Cross Contamination with Other Products

Details

Units Affected
672 90-count bottles
Distribution
U.S. Nationwide
Location
Mahwah, NJ

Frequently Asked Questions

What product was 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.. Recalled by Glenmark Pharmaceuticals Inc., USA. Units affected: 672 90-count bottles.
Why was this product recalled?
Cross Contamination with Other Products
Which agency issued this recall?
This recall was issued by the FDA Drug on December 17, 2025. Severity: Low. Recall number: D-0222-2026.