Potassium Acetate (Hospira, Inc.)
Welcome to the PulseAid listing for the Potassium Acetate drug offered from Hospira, Inc.. This Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [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: | POTASSIUM ACETATE |
| SUBSTANCE NAME: | POTASSIUM ACETATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2013-12-23 |
| END MARKETING DATE: | 0000-00-00 |
Potassium Acetate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Potassium Acetate from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 196.3(mg/mL) |
| START MARKETING DATE: | 2013-12-23 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-3294_535a901b-2ddb-4b2f-9428-3e62388801c2 |
| PRODUCT NDC: | 0409-3294 |
| APPLICATION NUMBER: | NDA018896 |
Other POTASSIUM ACETATE Pharmaceutical Manufacturers / Labelers:
