SYNDROS (Insys Therapeutics, Inc.)


Welcome to the PulseAid listing for the SYNDROS drug offered from Insys Therapeutics, Inc.. This Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient] 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: Insys Therapeutics, Inc.
NON-PROPRIETARY NAME: Dronabinol
SUBSTANCE NAME: DRONABINOL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Cannabinoid [EPC],Cannabinoids [Chemical/Ingredient]
ROUTE: ORAL
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2017-07-27
END MARKETING DATE: 0000-00-00


SYNDROS HUMAN PRESCRIPTION DRUG Details:

Item DescriptionSYNDROS from Insys Therapeutics, Inc.
LABELER NAME: Insys Therapeutics, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 5(mg/mL)
START MARKETING DATE: 2017-07-27
END MARKETING DATE: 0000-00-00
PRODUCT ID: 20482-335_40ab1c64-b842-4a71-baf4-eab1b5e365eb
PRODUCT NDC: 20482-335
APPLICATION NUMBER: NDA205525

Other DRONABINOL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
AbbVie Inc.Marinol
Actavis Pharma, Inc.Dronabinol
Akorn, Inc.Dronabinol
American Health PackagingDronabinol
Insys Therapeutics, Inc.SYNDROS
Mylan Pharmaceuticals Inc.Dronabinol
Par Pharmaceutical Inc.Dronabinol
Physicians Total Care, Inc.Dronabinol