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 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: | 2010-05-25 |
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: | 2(mg/1) |
START MARKETING DATE: | 2010-05-25 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0093-5378_a3dccdda-31a8-4b5c-a91b-62cc17473427 |
PRODUCT NDC: | 0093-5378 |
APPLICATION NUMBER: | ANDA090360 |
Other BUPRENORPHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: