"70121-1722-9" National Drug Code (NDC)

NDC Code	70121-1722-9
Package Description	24 POUCH in 1 CARTON (70121-1722-9) / 1 BAG in 1 POUCH / 250 mL in 1 BAG
Product NDC	70121-1722
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Phosphates
Non-Proprietary Name	Potassium Phosphates In Sodium Chloride
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	20240730
Marketing Category Name	NDA
Application Number	NDA218343
Manufacturer	Amneal Pharmaceuticals LLC
Substance Name	POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM PHOSPHATE, MONOBASIC
Strength	4.72; 4.48
Strength Unit	mg/mL; mg/mL
Pharmacy Classes	Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC]