Dacogen (Eisai Inc.)


Welcome to the PulseAid listing for the Dacogen drug offered from Eisai Inc.. This Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [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: Eisai Inc.
NON-PROPRIETARY NAME: decitabine
SUBSTANCE NAME: DECITABINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1996-05-03
END MARKETING DATE: 2018-12-31


Dacogen HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDacogen from Eisai Inc.
LABELER NAME: Eisai Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 50(mg/20mL)
START MARKETING DATE: 1996-05-03
END MARKETING DATE: 2018-12-31
PRODUCT ID: 62856-600_6c0cc062-642e-447b-a269-bc8e0f66be98
PRODUCT NDC: 62856-600
APPLICATION NUMBER: NDA021790

Other DECITABINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Accord Healthcare Inc.Decitabine
Dr.Reddy’s Laboratories IncDecitabine
Dr.Reddy’s Laboratories LimitedDecitabine
Eisai Inc.Dacogen
Otsuka America Pharmaceutical, Inc.Dacogen
Sandoz IncDecitabine