"62207-727-08" National Drug Code (NDC)

NDC Code	62207-727-08
Package Description	800 TABLET in 1 BOTTLE (62207-727-08)
Product NDC	62207-727
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride Extended-release
Non-Proprietary Name	Potassium Chloride Extended-release
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20210130
Marketing Category Name	ANDA
Application Number	ANDA214452
Manufacturer	Granules India Ltd
Substance Name	POTASSIUM CHLORIDE
Strength	1500
Strength Unit	mg/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]