Buprenorphine and Naloxone (Hi-Tech Pharmacal Co. Inc.)
Welcome to the PulseAid listing for the Buprenorphine and Naloxone drug offered from Hi-Tech Pharmacal Co. Inc.. This Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [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: | Hi-Tech Pharmacal Co. Inc. |
| NON-PROPRIETARY NAME: | buprenorphine hydrochloride and naloxone hydrochloride |
| SUBSTANCE NAME: | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| ROUTE: | SUBLINGUAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-01-07 |
| END MARKETING DATE: | 0000-00-00 |
Buprenorphine and Naloxone HUMAN PRESCRIPTION DRUG Details:
| Item Description | Buprenorphine and Naloxone from Hi-Tech Pharmacal Co. Inc. |
| LABELER NAME: | Hi-Tech Pharmacal Co. Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 8; 2(mg/1; mg/1) |
| START MARKETING DATE: | 2016-01-07 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50383-287_dd26b0f7-53cd-4c7b-b05c-9a7ce4174244 |
| PRODUCT NDC: | 50383-287 |
| APPLICATION NUMBER: | ANDA204431 |
Other BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
