NDC 59651-137
Nebivolol
Nebivolol
Nebivolol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is Nebivolol Hydrochloride.
| Product ID | 59651-137_6e43a4e2-574e-4f4a-804d-e346b4edd2f1 |
| NDC | 59651-137 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Nebivolol |
| Generic Name | Nebivolol |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-12-17 |
| Marketing Category | ANDA / |
| Application Number | ANDA211053 |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | NEBIVOLOL HYDROCHLORIDE |
| Active Ingredient Strength | 3 mg/1 |
| Pharm Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |