"72789-365-95" National Drug Code (NDC)

NDC Code	72789-365-95
Package Description	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-95)
Product NDC	72789-365
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride
Non-Proprietary Name	Potassium Chloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20231114
Marketing Category Name	ANDA
Application Number	ANDA076368
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	POTASSIUM CHLORIDE
Strength	20
Strength Unit	meq/1
Pharmacy Classes	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]