NDC 67877-392
Nebivolol
Nebivolol
Nebivolol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Ascend Laboratories, Llc. The primary component is Nebivolol Hydrochloride.
| Product ID | 67877-392_0f1472cb-fa10-4ad1-b5c4-bee8798e8078 |
| NDC | 67877-392 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Nebivolol |
| Generic Name | Nebivolol |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-09-16 |
| Marketing Category | ANDA / |
| Application Number | ANDA203828 |
| Labeler Name | Ascend Laboratories, LLC |
| Substance Name | NEBIVOLOL HYDROCHLORIDE |
| Active Ingredient Strength | 5 mg/1 |
| Pharm Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |