buprenorphine hydrochloride (PD-Rx Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the buprenorphine hydrochloride drug offered from PD-Rx 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: | PD-Rx Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | buprenorphine hydrochloride |
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: | 2010-09-24 |
END MARKETING DATE: | 0000-00-00 |
buprenorphine hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | buprenorphine hydrochloride from PD-Rx Pharmaceuticals, Inc. |
LABELER NAME: | PD-Rx Pharmaceuticals, Inc. |
DEA SCHEDULE: | CIII
|
ACTIVE STRENGTH: | 8(mg/1) |
START MARKETING DATE: | 2010-09-24 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 43063-667_5c3ad462-6a33-5d3b-e053-2991aa0a85d0 |
PRODUCT NDC: | 43063-667 |
APPLICATION NUMBER: | ANDA090622 |
Other BUPRENORPHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: