Ravicti (Hyperion Therapeutics, Inc.)


Welcome to the PulseAid listing for the Ravicti drug offered from Hyperion Therapeutics, Inc.. This 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: Hyperion Therapeutics, Inc.
NON-PROPRIETARY NAME: glycerol phenylbutyrate
SUBSTANCE NAME: GLYCEROL PHENYLBUTYRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-02-28
END MARKETING DATE: 0000-00-00


Ravicti HUMAN PRESCRIPTION DRUG Details:

Item DescriptionRavicti from Hyperion Therapeutics, Inc.
LABELER NAME: Hyperion Therapeutics, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1.1(g/mL)
START MARKETING DATE: 2013-02-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 76325-100_e3f10bc0-6ed9-11e2-bcfd-0800200c9a66
PRODUCT NDC: 76325-100
APPLICATION NUMBER: NDA203284

Other GLYCEROL PHENYLBUTYRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Horizon Therapeutics, LLC.Ravicti
Hyperion Therapeutics, Inc.Ravicti