Probuphine (Braeburn Pharmaceuticals)
Welcome to the PulseAid listing for the Probuphine drug offered from Braeburn Pharmaceuticals. This Partial Opioid Agonist [EPC],Partial 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: | Braeburn Pharmaceuticals |
NON-PROPRIETARY NAME: | buprenorphine hydrochloride |
SUBSTANCE NAME: | BUPRENORPHINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA] |
ROUTE: | SUBCUTANEOUS |
DOSAGE FORM: | IMPLANT |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2016-06-09 |
END MARKETING DATE: | 0000-00-00 |
Probuphine HUMAN PRESCRIPTION DRUG Details:
Item Description | Probuphine from Braeburn Pharmaceuticals |
LABELER NAME: | Braeburn Pharmaceuticals |
DEA SCHEDULE: | CIII
|
ACTIVE STRENGTH: | 80(mg/1) |
START MARKETING DATE: | 2016-06-09 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 58284-100_476d6991-1b02-4381-ba31-1bf5961477a8 |
PRODUCT NDC: | 58284-100 |
APPLICATION NUMBER: | NDA204442 |
Other BUPRENORPHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: