Byvalson (Allergan, Inc)


Welcome to the PulseAid listing for the Byvalson drug offered from Allergan, Inc. This Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Allergan, Inc
NON-PROPRIETARY NAME: nebivolol hydrochloride and valsartan
SUBSTANCE NAME: NEBIVOLOL HYDROCHLORIDE; VALSARTAN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2016-06-03
END MARKETING DATE: 0000-00-00


Byvalson HUMAN PRESCRIPTION DRUG Details:

Item DescriptionByvalson from Allergan, Inc
LABELER NAME: Allergan, Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 5; 80(mg/1; mg/1)
START MARKETING DATE: 2016-06-03
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0023-5874_12f03cb0-1ed2-45e8-b432-2ef5dcf4faa7
PRODUCT NDC: 0023-5874
APPLICATION NUMBER: NDA206302

Other NEBIVOLOL HYDROCHLORIDE; VALSARTAN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allergan, IncByvalson