Buprenorphine Hydrochloride Sublingual (Mylan Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Buprenorphine Hydrochloride Sublingual drug offered from Mylan Pharmaceuticals 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: | Mylan Pharmaceuticals Inc. |
| NON-PROPRIETARY NAME: | buprenorphine hydrochloride sublingual |
| 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: | 2015-03-06 |
| END MARKETING DATE: | 0000-00-00 |
Buprenorphine Hydrochloride Sublingual HUMAN PRESCRIPTION DRUG Details:
| Item Description | Buprenorphine Hydrochloride Sublingual from Mylan Pharmaceuticals Inc. |
| LABELER NAME: | Mylan Pharmaceuticals Inc. |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 2(mg/1) |
| START MARKETING DATE: | 2015-03-06 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0378-0923_851b6cdb-4be1-4b33-84e6-1e7af5fcd1aa |
| PRODUCT NDC: | 0378-0923 |
| APPLICATION NUMBER: | ANDA201066 |
Other BUPRENORPHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
