DEFITELIO (Jazz Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the DEFITELIO drug offered from Jazz Pharmaceuticals, Inc.. This 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: Jazz Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: defibrotide sodium
SUBSTANCE NAME: DEFIBROTIDE SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2016-03-30
END MARKETING DATE: 0000-00-00


DEFITELIO HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDEFITELIO from Jazz Pharmaceuticals, Inc.
LABELER NAME: Jazz Pharmaceuticals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 80(mg/mL)
START MARKETING DATE: 2016-03-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68727-800_c64466c2-3e9e-4470-96b7-0b25c3f0648f
PRODUCT NDC: 68727-800
APPLICATION NUMBER: NDA208114

Other DEFIBROTIDE SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Jazz Pharmaceuticals, Inc.DEFITELIO