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
70771-1599-0	70771-1599	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Lifesciences Limited	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1599-0)
70771-1599-1	70771-1599	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Lifesciences Limited	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1599-1)
70771-1600-0	70771-1600	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Lifesciences Limited	POTASSIUM CHLORIDE	1500 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-0)
70771-1600-1	70771-1600	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Lifesciences Limited	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-1)
70771-1600-5	70771-1600	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Lifesciences Limited	POTASSIUM CHLORIDE	1500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1600-5)
68382-861-01	68382-861	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Pharmaceuticals (USA) Inc.	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-861-01)
68382-861-10	68382-861	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Pharmaceuticals (USA) Inc.	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-861-10)
68382-740-01	68382-740	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Pharmaceuticals (USA) Inc.	POTASSIUM CHLORIDE	1500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-01)
68382-740-05	68382-740	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Pharmaceuticals (USA) Inc.	POTASSIUM CHLORIDE	1500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-05)
68382-740-10	68382-740	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, EXTENDED RELEASE	ORAL	20220203	N/A	ANDA	ANDA210395	Zydus Pharmaceuticals (USA) Inc.	POTASSIUM CHLORIDE	1500 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-740-10)