ZOHYDRO ER (Pernix Therapeutics)
Welcome to the PulseAid listing for the ZOHYDRO ER drug offered from Pernix Therapeutics. 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: | Pernix Therapeutics |
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 ER HUMAN PRESCRIPTION DRUG Details:
Item Description | ZOHYDRO ER from Pernix Therapeutics |
LABELER NAME: | Pernix Therapeutics |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 10(mg/1) |
START MARKETING DATE: | 2013-10-25 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 65224-310_42f646ec-e8c8-4790-82bf-56363124667f |
PRODUCT NDC: | 65224-310 |
APPLICATION NUMBER: | NDA202880 |
Other HYDROCODONE BITARTRATE Pharmaceutical Manufacturers / Labelers: