Buprenex (Reckitt Benckiser Pharmaceuticals Inc)
Welcome to the PulseAid listing for the Buprenex drug offered from Reckitt Benckiser Pharmaceuticals Inc. 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: | Reckitt Benckiser Pharmaceuticals Inc |
| NON-PROPRIETARY NAME: | buprenorphine hydrochloride |
| SUBSTANCE NAME: | BUPRENORPHINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
| DOSAGE FORM: | INJECTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1985-06-30 |
| END MARKETING DATE: | 0000-00-00 |
Buprenex HUMAN PRESCRIPTION DRUG Details:
| Item Description | Buprenex from Reckitt Benckiser Pharmaceuticals Inc |
| LABELER NAME: | Reckitt Benckiser Pharmaceuticals Inc |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 0.3(mg/mL) |
| START MARKETING DATE: | 1985-06-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 12496-0757_3837aa5b-dcf5-4c1b-bb37-b20882b9ddf5 |
| PRODUCT NDC: | 12496-0757 |
| APPLICATION NUMBER: | NDA018401 |
Other BUPRENORPHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
