Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Cross Contamination with Other Products
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.
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Reason CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso Nebivolol above acceptable intake (AI) limit.
Reason Failed Dissolution Specification; at the 6-month stability time point
Reason Failed Dissolution Specifications: Drug failed stage III dissolution testing.
Reason Failed Dissolution Specifications: One lot of product is being voluntarily recalled because dissolution test results failed to meet specification…
Reason Labeling: Label Mixup: NEBIVOLOL HCL, Tablet, 5 mg may have potentially been mislabeled as one of the following drugs: THYROID, Tablet, 30 mg, NDC…
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