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
0781-2855-05	0781-2855	HUMAN PRESCRIPTION DRUG	Ranitidine Hydrochloride	Ranitidine Hydrochloride	CAPSULE	ORAL	19971022	N/A	ANDA	ANDA074655	Sandoz Inc	RANITIDINE HYDROCHLORIDE	150 mg/1	500 CAPSULE in 1 BOTTLE (0781-2855-05)
0781-2855-31	0781-2855	HUMAN PRESCRIPTION DRUG	Ranitidine Hydrochloride	Ranitidine Hydrochloride	CAPSULE	ORAL	19971022	N/A	ANDA	ANDA074655	Sandoz Inc	RANITIDINE HYDROCHLORIDE	150 mg/1	30 CAPSULE in 1 BOTTLE (0781-2855-31)
0781-2855-60	0781-2855	HUMAN PRESCRIPTION DRUG	Ranitidine Hydrochloride	Ranitidine Hydrochloride	CAPSULE	ORAL	19971022	N/A	ANDA	ANDA074655	Sandoz Inc	RANITIDINE HYDROCHLORIDE	150 mg/1	60 CAPSULE in 1 BOTTLE (0781-2855-60)
0781-2855-92	0781-2855	HUMAN PRESCRIPTION DRUG	Ranitidine Hydrochloride	Ranitidine Hydrochloride	CAPSULE	ORAL	19971022	N/A	ANDA	ANDA074655	Sandoz Inc	RANITIDINE HYDROCHLORIDE	150 mg/1	90 CAPSULE in 1 BOTTLE (0781-2855-92)
0781-2865-05	0781-2865	HUMAN PRESCRIPTION DRUG	Ranitidine Hydrochloride	Ranitidine Hydrochloride	CAPSULE	ORAL	19971022	N/A	ANDA	ANDA074655	Sandoz Inc	RANITIDINE HYDROCHLORIDE	300 mg/1	500 CAPSULE in 1 BOTTLE (0781-2865-05)
0781-2865-31	0781-2865	HUMAN PRESCRIPTION DRUG	Ranitidine Hydrochloride	Ranitidine Hydrochloride	CAPSULE	ORAL	19971022	N/A	ANDA	ANDA074655	Sandoz Inc	RANITIDINE HYDROCHLORIDE	300 mg/1	30 CAPSULE in 1 BOTTLE (0781-2865-31)
0781-2865-92	0781-2865	HUMAN PRESCRIPTION DRUG	Ranitidine Hydrochloride	Ranitidine Hydrochloride	CAPSULE	ORAL	19971022	N/A	ANDA	ANDA074655	Sandoz Inc	RANITIDINE HYDROCHLORIDE	300 mg/1	90 CAPSULE in 1 BOTTLE (0781-2865-92)