"72789-001-30" National Drug Code (NDC)

NDC Code	72789-001-30
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-001-30)
Product NDC	72789-001
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	19981120
End Marketing Date	20211130
Marketing Category Name	ANDA
Application Number	ANDA074726
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	POTASSIUM CHLORIDE
Strength	750
Strength Unit	mg/1
Pharmacy Classes	Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]