"62037-710-01" National Drug Code (NDC)

NDC Code	62037-710-01
Package Description	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-710-01)
Product NDC	62037-710
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	20020410
Marketing Category Name	ANDA
Application Number	ANDA075604
Manufacturer	Actavis Pharma, Inc.
Substance Name	POTASSIUM CHLORIDE
Strength	10
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]