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 Description | ZUTRIPRO 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: