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
62207-727-43	62207-727	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET	ORAL	20210130	N/A	ANDA	ANDA214452	Granules India Ltd	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET in 1 BOTTLE (62207-727-43)
62207-727-47	62207-727	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET	ORAL	20210130	N/A	ANDA	ANDA214452	Granules India Ltd	POTASSIUM CHLORIDE	1500 mg/1	500 TABLET in 1 BOTTLE (62207-727-47)
62207-727-49	62207-727	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET	ORAL	20210625	N/A	ANDA	ANDA214452	Granules India Ltd	POTASSIUM CHLORIDE	1500 mg/1	1000 TABLET in 1 BOTTLE (62207-727-49)
62207-727-57	62207-727	HUMAN PRESCRIPTION DRUG	Potassium Chloride Extended-release	Potassium Chloride Extended-release	TABLET	ORAL	20210130	N/A	ANDA	ANDA214452	Granules India Ltd	POTASSIUM CHLORIDE	1500 mg/1	90 TABLET in 1 BOTTLE (62207-727-57)