NDC 68462-617
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 | 68462-617_cb47560d-9e35-4b0f-b12b-6ea478684a5b |
NDC | 68462-617 |
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 | 10 mg/1 |
Pharm Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |