Zubsolv (Orexo US, Inc.)
Welcome to the PulseAid listing for the Zubsolv drug offered from Orexo US, Inc.. This Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [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: | Orexo US, Inc. |
| NON-PROPRIETARY NAME: | buprenorphine hydrochloride and naloxone hydrochloride |
| SUBSTANCE NAME: | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| ROUTE: | SUBLINGUAL |
| DOSAGE FORM: | TABLET, ORALLY DISINTEGRATING |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2014-12-11 |
| END MARKETING DATE: | 0000-00-00 |
Zubsolv HUMAN PRESCRIPTION DRUG Details:
| Item Description | Zubsolv from Orexo US, Inc. |
| LABELER NAME: | Orexo US, Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 11.4; 2.9(mg/1; mg/1) |
| START MARKETING DATE: | 2014-12-11 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 54123-114_935430bb-7028-4f47-98ab-1c2145cecdcf |
| PRODUCT NDC: | 54123-114 |
| APPLICATION NUMBER: | NDA204242 |
Other BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
