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
82868-050-90	82868-050	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20240229	N/A	ANDA	ANDA216629	Northwind Pharmaceuticals, LLC	FUROSEMIDE	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (82868-050-90)
82868-050-30	82868-050	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20240229	N/A	ANDA	ANDA216629	Northwind Pharmaceuticals, LLC	FUROSEMIDE	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (82868-050-30)
42708-174-30	42708-174	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20230605	N/A	ANDA	ANDA216629	QPharma Inc	FUROSEMIDE	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (42708-174-30)
69844-051-01	69844-051	HUMAN PRESCRIPTION DRUG	furosemide	furosemide	TABLET	ORAL	20221017	N/A	ANDA	ANDA216629	Graviti Pharmaceuticals Private Limited	FUROSEMIDE	20 mg/1	50 TABLET in 1 BOTTLE (69844-051-01)
69844-051-02	69844-051	HUMAN PRESCRIPTION DRUG	furosemide	furosemide	TABLET	ORAL	20221017	N/A	ANDA	ANDA216629	Graviti Pharmaceuticals Private Limited	FUROSEMIDE	20 mg/1	100 TABLET in 1 BOTTLE (69844-051-02)
69844-051-03	69844-051	HUMAN PRESCRIPTION DRUG	furosemide	furosemide	TABLET	ORAL	20221017	N/A	ANDA	ANDA216629	Graviti Pharmaceuticals Private Limited	FUROSEMIDE	20 mg/1	1000 TABLET in 1 BOTTLE (69844-051-03)
69844-052-02	69844-052	HUMAN PRESCRIPTION DRUG	furosemide	furosemide	TABLET	ORAL	20221017	N/A	ANDA	ANDA216629	Graviti Pharmaceuticals Private Limited	FUROSEMIDE	40 mg/1	100 TABLET in 1 BOTTLE (69844-052-02)
69844-053-02	69844-053	HUMAN PRESCRIPTION DRUG	furosemide	furosemide	TABLET	ORAL	20221017	N/A	ANDA	ANDA216629	Graviti Pharmaceuticals Private Limited	FUROSEMIDE	80 mg/1	100 TABLET in 1 BOTTLE (69844-053-02)
69844-053-03	69844-053	HUMAN PRESCRIPTION DRUG	furosemide	furosemide	TABLET	ORAL	20221017	N/A	ANDA	ANDA216629	Graviti Pharmaceuticals Private Limited	FUROSEMIDE	80 mg/1	1000 TABLET in 1 BOTTLE (69844-053-03)
69844-052-03	69844-052	HUMAN PRESCRIPTION DRUG	furosemide	furosemide	TABLET	ORAL	20221017	N/A	ANDA	ANDA216629	Graviti Pharmaceuticals Private Limited	FUROSEMIDE	40 mg/1	1000 TABLET in 1 BOTTLE (69844-052-03)
69844-053-01	69844-053	HUMAN PRESCRIPTION DRUG	furosemide	furosemide	TABLET	ORAL	20221017	N/A	ANDA	ANDA216629	Graviti Pharmaceuticals Private Limited	FUROSEMIDE	80 mg/1	50 TABLET in 1 BOTTLE (69844-053-01)
69844-052-01	69844-052	HUMAN PRESCRIPTION DRUG	furosemide	furosemide	TABLET	ORAL	20221017	N/A	ANDA	ANDA216629	Graviti Pharmaceuticals Private Limited	FUROSEMIDE	40 mg/1	50 TABLET in 1 BOTTLE (69844-052-01)
50090-6642-0	50090-6642	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20230829	N/A	ANDA	ANDA216629	A-S Medication Solutions	FUROSEMIDE	20 mg/1	30 TABLET in 1 BOTTLE (50090-6642-0)
50090-6646-0	50090-6646	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20230829	N/A	ANDA	ANDA216629	A-S Medication Solutions	FUROSEMIDE	40 mg/1	30 TABLET in 1 BOTTLE (50090-6646-0)
50090-6646-1	50090-6646	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20230829	N/A	ANDA	ANDA216629	A-S Medication Solutions	FUROSEMIDE	40 mg/1	100 TABLET in 1 BOTTLE (50090-6646-1)
50090-6646-3	50090-6646	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20230829	N/A	ANDA	ANDA216629	A-S Medication Solutions	FUROSEMIDE	40 mg/1	60 TABLET in 1 BOTTLE (50090-6646-3)
50090-6646-9	50090-6646	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20230829	N/A	ANDA	ANDA216629	A-S Medication Solutions	FUROSEMIDE	40 mg/1	90 TABLET in 1 BOTTLE (50090-6646-9)
50090-6647-1	50090-6647	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20230829	N/A	ANDA	ANDA216629	A-S Medication Solutions	FUROSEMIDE	40 mg/1	180 TABLET in 1 BOTTLE (50090-6647-1)
50090-6642-1	50090-6642	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20230829	N/A	ANDA	ANDA216629	A-S Medication Solutions	FUROSEMIDE	20 mg/1	100 TABLET in 1 BOTTLE (50090-6642-1)
50090-6642-7	50090-6642	HUMAN PRESCRIPTION DRUG	Furosemide	Furosemide	TABLET	ORAL	20230829	N/A	ANDA	ANDA216629	A-S Medication Solutions	FUROSEMIDE	20 mg/1	200 TABLET in 1 BOTTLE (50090-6642-7)