Effervescent Potassium Chloride (Qualitest Pharmaceuticals)
Welcome to the PulseAid listing for the Effervescent Potassium Chloride drug offered from Qualitest Pharmaceuticals. 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],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: | Qualitest Pharmaceuticals |
| NON-PROPRIETARY NAME: | Potassium Bicarbonate and Potassium Chloride Effervescent Tablets for Oral Solution |
| SUBSTANCE NAME: | POTASSIUM CHLORIDE; LYSINE HYDROCHLORIDE; POTASSIUM BICARBONATE |
| 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],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: | ORAL |
| DOSAGE FORM: | TABLET, EFFERVESCENT |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2006-01-06 |
| END MARKETING DATE: | 0000-00-00 |
Effervescent Potassium Chloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Effervescent Potassium Chloride from Qualitest Pharmaceuticals |
| LABELER NAME: | Qualitest Pharmaceuticals |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1.25; 1.5; .7(g/1; g/1; g/1) |
| START MARKETING DATE: | 2006-01-06 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0603-3508_fc94a381-48f4-471f-be58-94e7924fd289 |
| PRODUCT NDC: | 0603-3508 |
| APPLICATION NUMBER: | |
Other POTASSIUM CHLORIDE; LYSINE HYDROCHLORIDE; POTASSIUM BICARBONATE Pharmaceutical Manufacturers / Labelers:
