Buphenyl (Horizon Pharma, Inc.)


Welcome to the PulseAid listing for the Buphenyl drug offered from Horizon Pharma, Inc.. This Ammonium Ion Binding Activity [MoA],Nitrogen Binding Agent [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: Horizon Pharma, Inc.
NON-PROPRIETARY NAME: sodium phenylbutyrate
SUBSTANCE NAME: SODIUM PHENYLBUTYRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Ammonium Ion Binding Activity [MoA],Nitrogen Binding Agent [EPC]
ROUTE: ORAL
DOSAGE FORM: POWDER
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1996-04-30
END MARKETING DATE: 0000-00-00


Buphenyl HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBuphenyl from Horizon Pharma, Inc.
LABELER NAME: Horizon Pharma, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.94(g/g)
START MARKETING DATE: 1996-04-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 75987-070_8b23789a-d8e5-4bdf-8a01-25b7ecd1d51d
PRODUCT NDC: 75987-070
APPLICATION NUMBER: NDA020573

Other SODIUM PHENYLBUTYRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Horizon Pharma, Inc.BUPHENYL
Mikart, Inc.sodium phenylbutyrate
Par Pharmaceutical, Inc.Sodium Phenylbutyrate
Sigmapharm Laboratories, LLCSodium Phenylbutyrate