"0615-8336-39" National Drug Code (NDC)

NDC Code	0615-8336-39
Package Description	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8336-39)
Product NDC	0615-8336
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	20160121
End Marketing Date	20220331
Marketing Category Name	ANDA
Application Number	ANDA206347
Manufacturer	NCS HealthCare of KY, LLC dba Vangard Labs
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]