Suboxone (Indivior Inc.)
Welcome to the PulseAid listing for the Suboxone drug offered from Indivior 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: | Indivior Inc. |
NON-PROPRIETARY NAME: | buprenorphine hydrochloride, 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: | FILM, SOLUBLE |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2010-09-13 |
END MARKETING DATE: | 0000-00-00 |
Suboxone HUMAN PRESCRIPTION DRUG Details:
Item Description | Suboxone from Indivior Inc. |
LABELER NAME: | Indivior Inc. |
DEA SCHEDULE: | CIII
|
ACTIVE STRENGTH: | 2; .5(mg/1; mg/1) |
START MARKETING DATE: | 2010-09-13 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 12496-1202_0f5a68db-888c-4348-a497-d657b5bb8888 |
PRODUCT NDC: | 12496-1202 |
APPLICATION NUMBER: | NDA022410 |
Other BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: