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
63187-333-30	63187-333	HUMAN PRESCRIPTION DRUG	Cimetidine	Cimetidine	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA074151	Proficient Rx LP	CIMETIDINE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-333-30)
50090-0500-1	50090-0500	HUMAN PRESCRIPTION DRUG	Cimetidine	Cimetidine	TABLET, FILM COATED	ORAL	20160726	N/A	ANDA	ANDA074151	A-S Medication Solutions	CIMETIDINE	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-0500-1)
50090-0500-0	50090-0500	HUMAN PRESCRIPTION DRUG	Cimetidine	Cimetidine	TABLET, FILM COATED	ORAL	20160629	N/A	ANDA	ANDA074151	A-S Medication Solutions	CIMETIDINE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-0500-0)
0093-8192-01	0093-8192	HUMAN PRESCRIPTION DRUG	Cimetidine	Cimetidine	TABLET, FILM COATED	ORAL	20031124	N/A	ANDA	ANDA074151	Teva Pharmaceuticals USA, Inc.	CIMETIDINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-8192-01)
0093-8192-05	0093-8192	HUMAN PRESCRIPTION DRUG	Cimetidine	Cimetidine	TABLET, FILM COATED	ORAL	20040128	N/A	ANDA	ANDA074151	Teva Pharmaceuticals USA, Inc.	CIMETIDINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-8192-05)
0093-8204-01	0093-8204	HUMAN PRESCRIPTION DRUG	Cimetidine	Cimetidine	TABLET, FILM COATED	ORAL	20040407	N/A	ANDA	ANDA074151	Teva Pharmaceuticals USA, Inc.	CIMETIDINE	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-8204-01)
0093-8204-05	0093-8204	HUMAN PRESCRIPTION DRUG	Cimetidine	Cimetidine	TABLET, FILM COATED	ORAL	20040202	N/A	ANDA	ANDA074151	Teva Pharmaceuticals USA, Inc.	CIMETIDINE	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-8204-05)
53002-3280-3	53002-3280	HUMAN PRESCRIPTION DRUG	Cimetidine	Cimetidine	TABLET, FILM COATED	ORAL	20221001	N/A	ANDA	ANDA074151	RPK Pharmaceuticals, Inc.	CIMETIDINE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-3280-3)