"68084-632-01" National Drug Code (NDC)

NDC Code	68084-632-01
Package Description	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-632-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-632-11)
Product NDC	68084-632
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	20130306
End Marketing Date	20240131
Marketing Category Name	ANDA
Application Number	ANDA075604
Manufacturer	American Health Packaging
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]