Buprenorphine (Sun Pharmaceutical Industries Limited)
Welcome to the PulseAid listing for the Buprenorphine drug offered from Sun Pharmaceutical Industries Limited. 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: | Sun Pharmaceutical Industries Limited |
| 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: | 2016-02-17 |
| END MARKETING DATE: | 0000-00-00 |
Buprenorphine HUMAN PRESCRIPTION DRUG Details:
| Item Description | Buprenorphine from Sun Pharmaceutical Industries Limited |
| LABELER NAME: | Sun Pharmaceutical Industries Limited |
| DEA SCHEDULE: | CIII
|
| ACTIVE STRENGTH: | 2(mg/1) |
| START MARKETING DATE: | 2016-02-17 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62756-459_7dbcac87-4f7f-4eee-aca2-0d5c4a14672a |
| PRODUCT NDC: | 62756-459 |
| APPLICATION NUMBER: | ANDA201760 |
Other BUPRENORPHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
