Dacogen (Otsuka America Pharmaceutical, Inc.)


Welcome to the PulseAid listing for the Dacogen drug offered from Otsuka America Pharmaceutical, 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: Otsuka America Pharmaceutical, 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: 0000-00-00


Dacogen HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDacogen from Otsuka America Pharmaceutical, Inc.
LABELER NAME: Otsuka America Pharmaceutical, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 50(mg/20mL)
START MARKETING DATE: 1996-05-03
END MARKETING DATE: 0000-00-00
PRODUCT ID: 59148-046_e1591080-2107-4acd-8f52-465a209cc1a9
PRODUCT NDC: 59148-046
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