ZUTRIPRO (Hawthorn Pharmaceuticals, Inc.)


Welcome to the PulseAid listing for the ZUTRIPRO drug offered from Hawthorn Pharmaceuticals, Inc.. This Opioid Agonist [EPC],Opioid Agonists [MoA],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [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: Hawthorn Pharmaceuticals, Inc.
NON-PROPRIETARY NAME: hydrocodone bitartrate, chlorpheniramine maleate, and pseudoephedrine hydrochloride
SUBSTANCE NAME: HYDROCODONE BITARTRATE; PSEUDOEPHEDRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Opioid Agonist [EPC],Opioid Agonists [MoA],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
ROUTE: ORAL
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2011-06-08
END MARKETING DATE: 0000-00-00


ZUTRIPRO HUMAN PRESCRIPTION DRUG Details:

Item DescriptionZUTRIPRO from Hawthorn Pharmaceuticals, Inc.
LABELER NAME: Hawthorn Pharmaceuticals, Inc.
DEA SCHEDULE: CII
ACTIVE STRENGTH: 5; 60; 4(mg/5mL; mg/5mL; mg/5mL)
START MARKETING DATE: 2011-06-08
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63717-876_e1431717-782c-4893-bf49-8e4c80713318
PRODUCT NDC: 63717-876
APPLICATION NUMBER: NDA022439

Other HYDROCODONE BITARTRATE; PSEUDOEPHEDRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Cypress Pharmaceutical, Inc.Hydrocodone Bitartrate, Chlorpheniramine Maleate, and Pseudoephedrine HCl
Hawthorn Pharmaceuticals, Inc.ZUTRIPRO