Potassium Chloride in Sodium Chloride (Hospira, Inc.)
Welcome to the PulseAid listing for the Potassium Chloride in Sodium Chloride drug offered from Hospira, Inc.. This Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],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: | SODIUM CHLORIDE and POTASSIUM CHLORIDE |
| SUBSTANCE NAME: | SODIUM CHLORIDE; POTASSIUM CHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],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 |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1988-10-17 |
| END MARKETING DATE: | 0000-00-00 |
Potassium Chloride in Sodium Chloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Potassium Chloride in Sodium Chloride from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 9; 1.49(g/1000mL; g/1000mL) |
| START MARKETING DATE: | 1988-10-17 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-7115_9b7424a1-6632-4609-a7dd-b4ed8703c3af |
| PRODUCT NDC: | 0409-7115 |
| APPLICATION NUMBER: | NDA019686 |
Other SODIUM CHLORIDE; POTASSIUM CHLORIDE Pharmaceutical Manufacturers / Labelers:
