DOBUTAMINE (Hospira, Inc.)
Welcome to the PulseAid listing for the DOBUTAMINE drug offered from Hospira, Inc.. This Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC] 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: | DOBUTAMINE |
| SUBSTANCE NAME: | DOBUTAMINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2005-06-29 |
| END MARKETING DATE: | 0000-00-00 |
DOBUTAMINE HUMAN PRESCRIPTION DRUG Details:
| Item Description | DOBUTAMINE from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 12.5(mg/mL) |
| START MARKETING DATE: | 2005-06-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-2344_1138db99-316b-42f4-b179-af580772748e |
| PRODUCT NDC: | 0409-2344 |
| APPLICATION NUMBER: | ANDA074086 |
Other DOBUTAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
