GaviLyte – N (GAVIS Pharmaceuticals, LLC)
Welcome to the PulseAid listing for the GaviLyte – N drug offered from GAVIS Pharmaceuticals, LLC. This Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],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: | GAVIS Pharmaceuticals, LLC |
| NON-PROPRIETARY NAME: | Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride and Sodium Bicarbonate |
| SUBSTANCE NAME: | POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],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: | POWDER, FOR SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2009-05-28 |
| END MARKETING DATE: | 0000-00-00 |
GaviLyte – N HUMAN PRESCRIPTION DRUG Details:
| Item Description | GaviLyte – N from GAVIS Pharmaceuticals, LLC |
| LABELER NAME: | GAVIS Pharmaceuticals, LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 420; 11.2; 5.72; 1.48(g/438.4g; g/438.4g; g/438.4g; g/438.4g) |
| START MARKETING DATE: | 2009-05-28 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 43386-050_9405ab30-a280-4968-a72f-ec9e25b293de |
| PRODUCT NDC: | 43386-050 |
| APPLICATION NUMBER: | ANDA090019 |
Other POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE Pharmaceutical Manufacturers / Labelers:
