GaviLyte GTM (GAVIS Pharmaceuticals, LLC)


Welcome to the PulseAid listing for the GaviLyte G 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],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 and Electrolytes
SUBSTANCE NAME: POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
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],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: 2009-06-01
END MARKETING DATE: 0000-00-00


GaviLyte G TM HUMAN PRESCRIPTION DRUG Details:

Item DescriptionGaviLyte G TM from GAVIS Pharmaceuticals, LLC
LABELER NAME: GAVIS Pharmaceuticals, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 236; 5.86; 6.74; 2.97; 22.74(g/274.31g; g/274.31g; g/274.31g; g/274.31g; g/274.31g)
START MARKETING DATE: 2009-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 43386-090_f252aead-84d7-4cb3-b968-a1bb351845ec
PRODUCT NDC: 43386-090
APPLICATION NUMBER: ANDA090231

Other POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; SODIUM SULFATE ANHYDROUS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GAVIS Pharmaceuticals, LLCGaviLyte – C
Novel Laboratories, Inc.Polyethylene Glycol-3350 and Electrolytes with Flavor Pack