amifostine (Bedford Laboratories)


Welcome to the PulseAid listing for the amifostine drug offered from Bedford Laboratories. This Cytoprotective Agent [EPC],Free Radical Scavenging 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: Bedford Laboratories
NON-PROPRIETARY NAME: amifostine
SUBSTANCE NAME: AMIFOSTINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Cytoprotective Agent [EPC],Free Radical Scavenging Activity [MoA]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2008-04-02
END MARKETING DATE: 2018-12-31


amifostine HUMAN PRESCRIPTION DRUG Details:

Item Descriptionamifostine from Bedford Laboratories
LABELER NAME: Bedford Laboratories
DEA SCHEDULE:
ACTIVE STRENGTH: 500(mg/10mL)
START MARKETING DATE: 2008-04-02
END MARKETING DATE: 2018-12-31
PRODUCT ID: 55390-308_5c68e9e1-47b8-4c03-8f8a-60afc67e023e
PRODUCT NDC: 55390-308
APPLICATION NUMBER: NDA020221

Other AMIFOSTINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bedford Laboratoriesamifostine
Cumberland Pharmaceuticals Inc.Ethyol
Sun Pharmaceutical Industries LimitedAMIFOSTINE