"33342-546-53" National Drug Code (NDC)

NDC Code	33342-546-53
Package Description	2 BOTTLE in 1 CARTON (33342-546-53) / 177 mL in 1 BOTTLE (33342-546-23)
Product NDC	33342-546
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sodium Sulfate, Potassium Sulfate And Magnesium Sulfate Oral
Non-Proprietary Name	Sodium Sulfate, Potassium Sulfate And Magnesium Sulfate Oral
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20260831
Marketing Category Name	ANDA
Application Number	ANDA219429
Manufacturer	Macleods Pharmaceuticals Limited
Substance Name	SODIUM SULFATE; POTASSIUM SULFATE; MAGNESIUM SULFATE
Strength	17.5; 3.13; 1.6
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]