"0517-2051-25" National Drug Code (NDC)

NDC Code	0517-2051-25
Package Description	25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2051-25) / 5 mL in 1 VIAL, SINGLE-DOSE (0517-2051-01)
Product NDC	0517-2051
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Phosphates
Non-Proprietary Name	Potassium Phosphates
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20231013
Marketing Category Name	ANDA
Application Number	ANDA216274
Manufacturer	American Regent, Inc.
Substance Name	POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM PHOSPHATE, MONOBASIC
Strength	236; 224
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]