Potassium Chloride in Dextrose and Sodium Chloride (Baxter Healthcare Corporation)
Welcome to the PulseAid listing for the Potassium Chloride in Dextrose and Sodium Chloride drug offered from Baxter Healthcare Corporation. 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: | Baxter Healthcare Corporation |
| NON-PROPRIETARY NAME: | Dextrose monohydrate, Sodium Chloride and Potassium Chloride |
| SUBSTANCE NAME: | DEXTROSE MONOHYDRATE; 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: | 1979-02-02 |
| END MARKETING DATE: | 0000-00-00 |
Potassium Chloride in Dextrose and Sodium Chloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Potassium Chloride in Dextrose and Sodium Chloride from Baxter Healthcare Corporation |
| LABELER NAME: | Baxter Healthcare Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5; 450; 75(g/100mL; mg/100mL; mg/100mL) |
| START MARKETING DATE: | 1979-02-02 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0338-6329_a5043890-7a8f-4718-bfc3-d20792d4bd61 |
| PRODUCT NDC: | 0338-6329 |
| APPLICATION NUMBER: | NDA018008 |
Other DEXTROSE MONOHYDRATE; SODIUM CHLORIDE; POTASSIUM CHLORIDE Pharmaceutical Manufacturers / Labelers:
