Venofer (American Regent, Inc.)


Welcome to the PulseAid listing for the Venofer drug offered from American Regent, 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: American Regent, Inc.
NON-PROPRIETARY NAME: iron sucrose
SUBSTANCE NAME: IRON SUCROSE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Iron [Chemical/Ingredient],Parenteral Iron Replacement [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2007-06-12
END MARKETING DATE: 0000-00-00


Venofer HUMAN PRESCRIPTION DRUG Details:

Item DescriptionVenofer from American Regent, Inc.
LABELER NAME: American Regent, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 20(mg/mL)
START MARKETING DATE: 2007-06-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0517-2310_cff8fa5e-41df-4fa6-b7f3-0c46168af38f
PRODUCT NDC: 0517-2310
APPLICATION NUMBER: NDA021135

Other IRON SUCROSE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
American Regent, Inc.Venofer
Fresenius Medical Care North AmericaVenofer
MARTIN EKWEALOR PHARMACEUTICALS, INC.Myferon 150