Bumetanide (Hospira, Inc.)
Welcome to the PulseAid listing for the Bumetanide drug offered from Hospira, Inc.. This Increased Diuresis at Loop of Henle [PE],Loop Diuretic [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: | BUMETANIDE |
| SUBSTANCE NAME: | BUMETANIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2006-07-06 |
| END MARKETING DATE: | 0000-00-00 |
Bumetanide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Bumetanide from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.25(mg/mL) |
| START MARKETING DATE: | 2006-07-06 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-1412_3b8bcc6b-8a49-419a-b420-ed4d5200dd78 |
| PRODUCT NDC: | 0409-1412 |
| APPLICATION NUMBER: | ANDA074332 |
Other BUMETANIDE Pharmaceutical Manufacturers / Labelers:
