Buprenorphine (Actavis Pharma, Inc.)
Welcome to the PulseAid listing for the Buprenorphine drug offered from Actavis Pharma, 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: | Actavis Pharma, 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: | SUBLINGUAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2015-04-10 |
| END MARKETING DATE: | 0000-00-00 |
Buprenorphine HUMAN PRESCRIPTION DRUG Details:
| Item Description | Buprenorphine from Actavis Pharma, Inc. |
| LABELER NAME: | Actavis Pharma, Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 8(mg/1) |
| START MARKETING DATE: | 2015-04-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0228-3153_7456fa8b-1147-49af-8fe6-906ad574413f |
| PRODUCT NDC: | 0228-3153 |
| APPLICATION NUMBER: | ANDA090819 |
Other BUPRENORPHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
