DOPamine HYDROCHLORIDE AND DEXTROSE (Hospira, Inc.)
Welcome to the PulseAid listing for the DOPamine HYDROCHLORIDE AND DEXTROSE drug offered from Hospira, Inc.. This Catecholamine [EPC],Catecholamines [Chemical/Ingredient] 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: | DOPamine HYDROCHLORIDE AND DEXTROSE |
SUBSTANCE NAME: | DOPAMINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1981-05-19 |
END MARKETING DATE: | 0000-00-00 |
DOPamine HYDROCHLORIDE AND DEXTROSE HUMAN PRESCRIPTION DRUG Details:
Item Description | DOPamine HYDROCHLORIDE AND DEXTROSE from Hospira, Inc. |
LABELER NAME: | Hospira, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 160(mg/100mL) |
START MARKETING DATE: | 1981-05-19 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0409-4142_5a40978d-afc5-4f6f-8658-f34890a4011c |
PRODUCT NDC: | 0409-4142 |
APPLICATION NUMBER: | NDA018132 |
Other DOPAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: