Buprenorphine (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Buprenorphine drug offered from Teva Pharmaceuticals USA, 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: | Teva Pharmaceuticals USA, Inc. |
| NON-PROPRIETARY NAME: | Buprenorphine |
| SUBSTANCE NAME: | BUPRENORPHINE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA] |
| ROUTE: | TRANSDERMAL |
| DOSAGE FORM: | PATCH, EXTENDED RELEASE |
| MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
| START MARKETING DATE: | 2017-05-30 |
| END MARKETING DATE: | 0000-00-00 |
Buprenorphine HUMAN PRESCRIPTION DRUG Details:
| Item Description | Buprenorphine from Teva Pharmaceuticals USA, Inc. |
| LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 5(ug/h) |
| START MARKETING DATE: | 2017-05-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0093-3600_6f01f14e-5b47-4544-9656-d471cebe03ee |
| PRODUCT NDC: | 0093-3600 |
| APPLICATION NUMBER: | NDA021306 |
Other BUPRENORPHINE Pharmaceutical Manufacturers / Labelers:
