"72789-002-30" National Drug Code (NDC)

NDC Code	72789-002-30
Package Description	30 CAPSULE in 1 BOTTLE, PLASTIC (72789-002-30)
Product NDC	72789-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride
Proprietary Name Suffix	Extended Release
Non-Proprietary Name	Potassium Chloride
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20180401
Marketing Category Name	ANDA
Application Number	ANDA208864
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	POTASSIUM CHLORIDE
Strength	750
Strength Unit	mg/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]