Buprenorphine Hydrochloride (Hospira, Inc.)
Welcome to the PulseAid listing for the Buprenorphine Hydrochloride drug offered from Hospira, 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: | Hospira, 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: | INTRAMUSCULAR; INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2005-06-14 |
END MARKETING DATE: | 0000-00-00 |
Buprenorphine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Buprenorphine Hydrochloride from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: | CIII
|
ACTIVE STRENGTH: | 0.3(mg/mL) |
START MARKETING DATE: | 2005-06-14 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0409-2012_3f59ad84-8359-4e75-854d-0e6d641590f4 |
PRODUCT NDC: | 0409-2012 |
APPLICATION NUMBER: | ANDA074137 |
Other BUPRENORPHINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: