Potassium Chloride in Sodium Chloride (Baxter Healthcare Corporation)
Welcome to the PulseAid listing for the Potassium Chloride in 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: | Potassium Chloride and Sodium 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: | 1979-02-02 |
END MARKETING DATE: | 0000-00-00 |
Potassium Chloride in Sodium Chloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Potassium Chloride in Sodium Chloride from Baxter Healthcare Corporation |
LABELER NAME: | Baxter Healthcare Corporation |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 900; 150(mg/100mL; mg/100mL) |
START MARKETING DATE: | 1979-02-02 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0338-0691_5ab0219a-78af-4911-a982-1bafc97db420 |
PRODUCT NDC: | 0338-0691 |
APPLICATION NUMBER: | NDA017648 |
Other SODIUM CHLORIDE; POTASSIUM CHLORIDE Pharmaceutical Manufacturers / Labelers: