NDC 72241-035
Nebivolol
Nebivolol
Nebivolol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Modavar Pharmaceuticals Llc. The primary component is Nebivolol Hydrochloride.
| Product ID | 72241-035_19d20396-ade8-400e-94f4-69913637d051 |
| NDC | 72241-035 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Nebivolol |
| Generic Name | Nebivolol |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2017-12-29 |
| Marketing Category | ANDA / |
| Application Number | ANDA208717 |
| Labeler Name | Modavar Pharmaceuticals LLC |
| Substance Name | NEBIVOLOL HYDROCHLORIDE |
| Active Ingredient Strength | 20 mg/1 |
| Pharm Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |