DOPamine Hydrochloride (Hospira, Inc.)
Welcome to the PulseAid listing for the DOPamine Hydrochloride 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 |
| SUBSTANCE NAME: | DOPAMINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1981-05-19 |
| END MARKETING DATE: | 0000-00-00 |
DOPamine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | DOPamine Hydrochloride from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 80(mg/mL) |
| START MARKETING DATE: | 1981-05-19 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-4265_6055eb0c-5c9f-423c-b36e-d3e96738e3bb |
| PRODUCT NDC: | 0409-4265 |
| APPLICATION NUMBER: | NDA018132 |
Other DOPAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
