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
70436-153-02	70436-153	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200201	N/A	ANDA	ANDA212561	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	1500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-153-02)
70436-153-01	70436-153	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200201	N/A	ANDA	ANDA212561	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-153-01)
70436-152-03	70436-152	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200201	N/A	ANDA	ANDA212561	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-152-03)
70436-152-01	70436-152	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200201	N/A	ANDA	ANDA212561	Slate Run Pharmaceuticals, LLC	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-152-01)