CONTRAVE (Takeda Pharmaceuticals America, Inc.)
Welcome to the PulseAid listing for the CONTRAVE drug offered from Takeda Pharmaceuticals America, Inc.. This Opioid Antagonist [EPC],Opioid Antagonists [MoA],Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [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: | Takeda Pharmaceuticals America, Inc. |
NON-PROPRIETARY NAME: | naltrexone hydrochloride and bupropion hydrochloride |
SUBSTANCE NAME: | NALTREXONE HYDROCHLORIDE; BUPROPION HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Opioid Antagonist [EPC],Opioid Antagonists [MoA],Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2014-09-10 |
END MARKETING DATE: | 0000-00-00 |
CONTRAVE HUMAN PRESCRIPTION DRUG Details:
Item Description | CONTRAVE from Takeda Pharmaceuticals America, Inc. |
LABELER NAME: | Takeda Pharmaceuticals America, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 8; 90(mg/1; mg/1) |
START MARKETING DATE: | 2014-09-10 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 64764-890_ed2da3a6-0614-4bea-8e82-962cbaae6428 |
PRODUCT NDC: | 64764-890 |
APPLICATION NUMBER: | NDA200063 |
Other NALTREXONE HYDROCHLORIDE; BUPROPION HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: