FDAFDA · Food and drugs·Recall number D-0222-2026
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.
Published December 17, 2025 · Recall initiated: November 18, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Cross Contamination with Other Products
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- NEBIVOLOL
- Manufacturer
- Glenmark Pharmaceuticals Inc., USA
- Distributor
- U.S. Nationwide
- UPC
- 0342291872905
- Lot
- Lot# 17240988; Exp. 05/31/2026
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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