Auryxia (Keryx Biopharmaceuticals, Inc.)


Welcome to the PulseAid listing for the Auryxia drug offered from Keryx Biopharmaceuticals, Inc.. This Iron [Chemical/Ingredient],Parenteral Iron Replacement [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA] 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: Keryx Biopharmaceuticals, Inc.
NON-PROPRIETARY NAME: ferric citrate
SUBSTANCE NAME: TETRAFERRIC TRICITRATE DECAHYDRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Iron [Chemical/Ingredient],Parenteral Iron Replacement [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2014-09-17
END MARKETING DATE: 0000-00-00


Auryxia HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAuryxia from Keryx Biopharmaceuticals, Inc.
LABELER NAME: Keryx Biopharmaceuticals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 210(mg/1)
START MARKETING DATE: 2014-09-17
END MARKETING DATE: 0000-00-00
PRODUCT ID: 59922-631_fec0ab98-d8ba-45c2-9017-ca1407116872
PRODUCT NDC: 59922-631
APPLICATION NUMBER: NDA205874

Other TETRAFERRIC TRICITRATE DECAHYDRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Keryx Biopharmaceuticals, Inc.Auryxia