"42291-672-90" National Drug Code (NDC)

NDC Code	42291-672-90
Package Description	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-672-90)
Product NDC	42291-672
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	20140507
Marketing Category Name	ANDA
Application Number	ANDA076368
Manufacturer	AvKARE, Inc.
Substance Name	POTASSIUM CHLORIDE
Strength	20
Strength Unit	meq/1
Pharmacy Classes	Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]