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
50090-5335-0	50090-5335	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201104	N/A	ANDA	ANDA210921	A-S Medication Solutions	POTASSIUM CHLORIDE	750 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-0)
50090-5335-1	50090-5335	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201104	N/A	ANDA	ANDA210921	A-S Medication Solutions	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-1)
50090-5335-2	50090-5335	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201104	N/A	ANDA	ANDA210921	A-S Medication Solutions	POTASSIUM CHLORIDE	750 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-2)
50090-5335-3	50090-5335	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201104	N/A	ANDA	ANDA210921	A-S Medication Solutions	POTASSIUM CHLORIDE	750 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-3)
65862-986-01	65862-986	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	600 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-01)
65862-986-05	65862-986	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	600 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-986-05)
65862-986-12	65862-986	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	600 mg/1	120 BLISTER PACK in 1 CARTON (65862-986-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-06)
65862-986-80	65862-986	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	600 mg/1	80 BLISTER PACK in 1 CARTON (65862-986-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-986-04)
65862-987-01	65862-987	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	750 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-01)
65862-987-12	65862-987	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	750 mg/1	120 BLISTER PACK in 1 CARTON (65862-987-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-06)
65862-987-80	65862-987	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	750 mg/1	80 BLISTER PACK in 1 CARTON (65862-987-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-04)
65862-987-99	65862-987	HUMAN PRESCRIPTION DRUG	Potassium Chloride	Potassium Chloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181219	N/A	ANDA	ANDA210921	Aurobindo Pharma Limited	POTASSIUM CHLORIDE	750 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-99)