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Class III: unlikely to cause harmOngoing

Glenmark Pharmaceuticals Nebivolol Tablets Recall

Nebivolol Tablets, 20 mg, 90 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceutical…

Glenmark Pharmaceuticals Inc., USA · Mahwah, NJ

Risk level
Class III
Reported by FDA
Dec 17, 2025
Recall ID
D-0222-2026
Check your lot numberHow we source this data

Summary

Glenmark Pharmaceuticals recalled Nebivolol Tablets starting Nov 18, 2025. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0222-2026 on Dec 17, 2025. Reason: Cross Contamination with Other Products. Status: Ongoing.

Why it was recalled

Cross Contamination with Other Products

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.

Lot numbers, UPCs & expiration codes

Lot# 17240988; Exp. 05/31/2026

Where it was sold

U.S. Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0222-2026
Classification
Class III
Status
Ongoing
Recall initiated
Nov 18, 2025
FDA report date
Dec 17, 2025
Quantity
672 90-count bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Glenmark Pharmaceuticals Inc., USA

Original FDA data

Every field from FDA enforcement report D-0222-2026, exactly as published.

Show all FDA fields
City
Mahwah
State
NJ
Status
Ongoing
Country
United States
Event ID
98014
Address
750 Corporate Dr
Code information
Lot# 17240988; Exp. 05/31/2026
Postal code
07430-2009
Report date
Dec 17, 2025
Product type
Drugs
Recall number
D-0222-2026
Classification
Class III
Recalling firm
Glenmark Pharmaceuticals Inc., USA
Product quantity
672 90-count bottles
Reason for recall
Cross Contamination with Other Products
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
U.S. Nationwide
Recall initiation date
Nov 18, 2025
Initial firm notification
Letter
Center classification date
Dec 9, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0222-2026, published Dec 17, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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