Buprenorphine Hydrochloride (American Regent, Inc.)
Welcome to the PulseAid listing for the Buprenorphine Hydrochloride drug offered from American Regent, 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: | American Regent, 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, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2010-08-13 |
| END MARKETING DATE: | 0000-00-00 |
Buprenorphine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Buprenorphine Hydrochloride from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 0.324(mg/mL) |
| START MARKETING DATE: | 2010-08-13 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-0725_2cb6acc4-4f84-4433-bfd1-2ffe35faf3e9 |
| PRODUCT NDC: | 0517-0725 |
| APPLICATION NUMBER: | ANDA078331 |
Other BUPRENORPHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
