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
63561-0165-1	63561-0165	HUMAN PRESCRIPTION DRUG	Furosemide	FUROSEMIDE	TABLET	ORAL	20260115	N/A	NDA	NDA018569	Granulation Technology, Inc.	FUROSEMIDE	40 mg/1	100 TABLET in 1 BOTTLE (63561-0165-1)
63561-0165-2	63561-0165	HUMAN PRESCRIPTION DRUG	Furosemide	FUROSEMIDE	TABLET	ORAL	20251218	N/A	NDA	NDA018569	Granulation Technology, Inc.	FUROSEMIDE	40 mg/1	1000 TABLET in 1 BOTTLE (63561-0165-2)
63561-0165-9	63561-0165	HUMAN PRESCRIPTION DRUG	Furosemide	FUROSEMIDE	TABLET	ORAL	20251218	N/A	NDA	NDA018569	Granulation Technology, Inc.	FUROSEMIDE	40 mg/1	90 TABLET in 1 BOTTLE (63561-0165-9)
63561-0166-1	63561-0166	HUMAN PRESCRIPTION DRUG	Furosemide	FUROSEMIDE	TABLET	ORAL	20260115	N/A	NDA	NDA018569	Granulation Technology, Inc.	FUROSEMIDE	80 mg/1	100 TABLET in 1 BOTTLE (63561-0166-1)
63561-0166-5	63561-0166	HUMAN PRESCRIPTION DRUG	Furosemide	FUROSEMIDE	TABLET	ORAL	20251218	N/A	NDA	NDA018569	Granulation Technology, Inc.	FUROSEMIDE	80 mg/1	500 TABLET in 1 BOTTLE (63561-0166-5)
63561-0166-9	63561-0166	HUMAN PRESCRIPTION DRUG	Furosemide	FUROSEMIDE	TABLET	ORAL	20251218	N/A	NDA	NDA018569	Granulation Technology, Inc.	FUROSEMIDE	80 mg/1	90 TABLET in 1 BOTTLE (63561-0166-9)
63561-0164-9	63561-0164	HUMAN PRESCRIPTION DRUG	Furosemide	FUROSEMIDE	TABLET	ORAL	20251218	N/A	NDA	NDA018569	Granulation Technology, Inc.	FUROSEMIDE	20 mg/1	90 TABLET in 1 BOTTLE (63561-0164-9)
63561-0164-2	63561-0164	HUMAN PRESCRIPTION DRUG	Furosemide	FUROSEMIDE	TABLET	ORAL	20251218	N/A	NDA	NDA018569	Granulation Technology, Inc.	FUROSEMIDE	20 mg/1	1000 TABLET in 1 BOTTLE (63561-0164-2)
63561-0164-1	63561-0164	HUMAN PRESCRIPTION DRUG	Furosemide	FUROSEMIDE	TABLET	ORAL	20260115	N/A	NDA	NDA018569	Granulation Technology, Inc.	FUROSEMIDE	20 mg/1	100 TABLET in 1 BOTTLE (63561-0164-1)