"67877-725-92" National Drug Code (NDC)

NDC Code	67877-725-92
Package Description	2 BOTTLE, PLASTIC in 1 CARTON (67877-725-92) / 177 mL in 1 BOTTLE, PLASTIC
Product NDC	67877-725
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sodium Sulfate, Potassium Sulfate And Magnesium Sulfate
Non-Proprietary Name	Sodium Sulfate, Potassium Sulfate And Magnesium Sulfate
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20240329
Marketing Category Name	ANDA
Application Number	ANDA213924
Manufacturer	Ascend Laboratories, LLC
Substance Name	MAGNESIUM SULFATE, UNSPECIFIED FORM; POTASSIUM SULFATE; SODIUM SULFATE
Strength	1.6; 3.13; 17.5
Strength Unit	g/177mL; g/177mL; g/177mL
Pharmacy Classes	Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]