NDC 68462-618
nebivolol
Nebivolol Hydrochloride
nebivolol is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Glenmark Pharmaceuticals Inc., Usa. The primary component is Nebivolol Hydrochloride.
| Product ID | 68462-618_cb47560d-9e35-4b0f-b12b-6ea478684a5b |
| NDC | 68462-618 |
| Product Type | Human Prescription Drug |
| Proprietary Name | nebivolol |
| Generic Name | Nebivolol Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2017-05-25 |
| Marketing Category | ANDA / |
| Application Number | ANDA203821 |
| Labeler Name | Glenmark Pharmaceuticals Inc., USA |
| 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 |