NDC 0904-7190
nebivolol
Nebivolol
nebivolol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Major Pharmaceuticals. The primary component is Nebivolol Hydrochloride.
| Product ID | 0904-7190_13c6911b-c653-4fa9-87ea-3e505bf3ba34 |
| NDC | 0904-7190 |
| Product Type | Human Prescription Drug |
| Proprietary Name | nebivolol |
| Generic Name | Nebivolol |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2018-03-02 |
| Marketing Category | ANDA / |
| Application Number | ANDA203966 |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | NEBIVOLOL HYDROCHLORIDE |
| Active Ingredient Strength | 10 mg/1 |
| Pharm Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |