NDC 59651-140 – Nebivolol
Nebivolol Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC59651-140
Product details
- Brand name
- Nebivolol
- Generic name
- Nebivolol
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA211053
- Marketed since
- December 17, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Nebivolol Hydrochloride 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 59651-140-30 | 30 TABLET in 1 BOTTLE (59651-140-30) | Dec 17, 2021 |
| 59651-140-90 | 90 TABLET in 1 BOTTLE (59651-140-90) | Dec 17, 2021 |
Recalls mentioning this NDC
- D-0149-2025 Dec 25, 2024 · Class II
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso Nebivolol above acceptable intake (AI) limit.
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