美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
63629-8442-1	63629-8442	HUMAN PRESCRIPTION DRUG	Potassium chloride extended release	Potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20151218	N/A	ANDA	ANDA205993	Bryant Ranch Prepack	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8442-1)
55154-6709-0	55154-6709	HUMAN PRESCRIPTION DRUG	Potassium chloride extended release	Potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160505	N/A	ANDA	ANDA205993	Cardinal Health 107, LLC	POTASSIUM CHLORIDE	10 meq/1	10 BLISTER PACK in 1 BAG (55154-6709-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0574-0275-11	0574-0275	HUMAN PRESCRIPTION DRUG	Potassium chloride extended release	Potassium chloride	TABLET, EXTENDED RELEASE	ORAL	20160505	N/A	ANDA	ANDA205993	Padagis US LLC	POTASSIUM CHLORIDE	750 mg/1	10 BLISTER PACK in 1 BOX, UNIT-DOSE (0574-0275-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK