Class II ยท Moderate risk
Nebivolol Tablets
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso Nebivolol above acceptable intake (AI) limit.
National Drug Code
Is NDC 59651-0137-30 recalled?
Nebivolol · 30 TABLET in 1 BOTTLE (59651-137-30)
Yes — this exact package was recalled
1 FDA recall names the code 59651-0137-30 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Nebivolol
- Strength
- NEBIVOLOL HYDROCHLORIDE 2.5 mg/1
- Form
- Tablet · Oral
- Labeler
- Aurobindo Pharma Limited
- Type
- Human Prescription Drug
- Product code
- 59651-0137
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 59651-0144 See recall 2
- 59651-0032 Ibuprofen 1
- 59651-0104 Eletriptan Hydrobromide 1
- 59651-0145 See recall 1
- 59651-0616 Rufinamide 1
- 59651-0617 Rufinamide 1
Free recall alerts
Know the day your medication is recalled
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