"24338-175-01" National Drug Code (NDC)

NDC Code	24338-175-01
Package Description	2 BOTTLE, PLASTIC in 1 CARTON (24338-175-01) / 177.4 mL in 1 BOTTLE, PLASTIC
Product NDC	24338-175
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Suprep Bowel Prep
Non-Proprietary Name	Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
Dosage Form	SOLUTION, CONCENTRATE
Usage	ORAL
Start Marketing Date	20260401
Marketing Category Name	NDA
Application Number	NDA022372
Manufacturer	Azurity Pharmaceuticals, Inc.
Substance Name	MAGNESIUM SULFATE, UNSPECIFIED FORM; POTASSIUM SULFATE; SODIUM SULFATE
Strength	1.6; 3.13; 17.5
Strength Unit	g/mL; g/mL; g/mL
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]