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
50090-4734-9	50090-4734	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	CAPSULE, COATED, EXTENDED RELEASE	ORAL	20191119	N/A	ANDA	ANDA203002	A-S Medication Solutions	POTASSIUM CHLORIDE	10 meq/1	90 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4734-9)
68180-799-01	68180-799	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	CAPSULE, COATED, EXTENDED RELEASE	ORAL	20160525	20260430	ANDA	ANDA203002	Lupin Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	10 meq/1	100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68180-799-01)
68180-799-02	68180-799	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	CAPSULE, COATED, EXTENDED RELEASE	ORAL	20160304	20260430	ANDA	ANDA203002	Lupin Pharmaceuticals, Inc.	POTASSIUM CHLORIDE	10 meq/1	500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (68180-799-02)
57297-799-01	57297-799	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	CAPSULE, COATED, EXTENDED RELEASE	ORAL	20160525	20260430	ANDA	ANDA203002	LUPIN LIMITED	POTASSIUM CHLORIDE	10 meq/1	100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-01)
57297-799-02	57297-799	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	CAPSULE, COATED, EXTENDED RELEASE	ORAL	20160304	20260430	ANDA	ANDA203002	LUPIN LIMITED	POTASSIUM CHLORIDE	10 meq/1	500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-02)
57297-799-03	57297-799	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	CAPSULE, COATED, EXTENDED RELEASE	ORAL	20160525	20260430	ANDA	ANDA203002	LUPIN LIMITED	POTASSIUM CHLORIDE	10 meq/1	1000 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (57297-799-03)