"55289-738-30" National Drug Code (NDC)

NDC Code	55289-738-30
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-738-30)
Product NDC	55289-738
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	20040818
End Marketing Date	20240229
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]