"62037-999-10" National Drug Code (NDC)

NDC Code	62037-999-10
Package Description	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-999-10)
Product NDC	62037-999
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	20240831
Marketing Category Name	ANDA
Application Number	ANDA076368
Manufacturer	Actavis Pharma, 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]