Byvalson is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Allergan, Inc.. The primary component is Nebivolol Hydrochloride; Valsartan.
Product ID | 0023-5874_6964c0d8-8223-4992-b42c-43d3de03080e |
NDC | 0023-5874 |
Product Type | Human Prescription Drug |
Proprietary Name | Byvalson |
Generic Name | Nebivolol Hydrochloride And Valsartan |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 2016-06-03 |
Marketing Category | NDA / NDA |
Application Number | NDA206302 |
Labeler Name | Allergan, Inc. |
Substance Name | NEBIVOLOL HYDROCHLORIDE; VALSARTAN |
Active Ingredient Strength | 5 mg/1; mg/1 |
Pharm Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2016-06-03 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA206302 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-06-03 |
Marketing End Date | 2019-05-31 |
Marketing Category | NDA |
Application Number | NDA206302 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-06-03 |
Marketing End Date | 2019-05-31 |
Marketing Category | NDA |
Application Number | NDA206302 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-06-03 |
Marketing End Date | 2019-05-31 |
Marketing Category | NDA |
Application Number | NDA206302 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-06-03 |
Marketing End Date | 2019-05-31 |
Marketing Category | NDA |
Application Number | NDA206302 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2016-06-03 |
Marketing End Date | 2019-05-31 |
Marketing Category | NDA |
Application Number | NDA206302 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2016-06-03 |
Marketing End Date | 2019-05-31 |
Ingredient | Strength |
---|---|
NEBIVOLOL HYDROCHLORIDE | 5 mg/1 |
SPL SET ID: | b4ad6a5b-e69d-4b39-9fe3-58569a964978 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BYVALSON 86101968 5073605 Live/Registered |
ALLERGAN SALES, LLC 2013-10-25 |