Zohydro (Zogenix, Inc.)


Welcome to the PulseAid listing for the Zohydro drug offered from Zogenix, Inc.. This Opioid Agonist [EPC],Opioid Agonists [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: Zogenix, Inc.
NON-PROPRIETARY NAME: hydrocodone bitartrate
SUBSTANCE NAME: HYDROCODONE BITARTRATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Opioid Agonist [EPC],Opioid Agonists [MoA]
ROUTE: ORAL
DOSAGE FORM: CAPSULE, EXTENDED RELEASE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-10-25
END MARKETING DATE: 0000-00-00


Zohydro HUMAN PRESCRIPTION DRUG Details:

Item DescriptionZohydro from Zogenix, Inc.
LABELER NAME: Zogenix, Inc.
DEA SCHEDULE: CII
ACTIVE STRENGTH: 10(mg/1)
START MARKETING DATE: 2013-10-25
END MARKETING DATE: 0000-00-00
PRODUCT ID: 43376-210_78f08950-950a-49a4-bd99-3f23befa4d01
PRODUCT NDC: 43376-210
APPLICATION NUMBER: NDA202880

Other HYDROCODONE BITARTRATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Pernix TherapeuticsZOHYDRO ER
Purdue Pharma LPHysingla ER
Zogenix, Inc.Zohydro