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
53746-253-01	53746-253	HUMAN PRESCRIPTION DRUG	Ranitidine	Ranitidine	TABLET	ORAL	20091216	N/A	ANDA	ANDA077824	Amneal Pharmaceuticals of New York LLC	RANITIDINE HYDROCHLORIDE	150 mg/1	100 TABLET in 1 BOTTLE (53746-253-01)
53746-253-05	53746-253	HUMAN PRESCRIPTION DRUG	Ranitidine	Ranitidine	TABLET	ORAL	20091216	N/A	ANDA	ANDA077824	Amneal Pharmaceuticals of New York LLC	RANITIDINE HYDROCHLORIDE	150 mg/1	500 TABLET in 1 BOTTLE (53746-253-05)
53746-253-10	53746-253	HUMAN PRESCRIPTION DRUG	Ranitidine	Ranitidine	TABLET	ORAL	20091216	N/A	ANDA	ANDA077824	Amneal Pharmaceuticals of New York LLC	RANITIDINE HYDROCHLORIDE	150 mg/1	1000 TABLET in 1 BOTTLE (53746-253-10)
53746-253-18	53746-253	HUMAN PRESCRIPTION DRUG	Ranitidine	Ranitidine	TABLET	ORAL	20091216	N/A	ANDA	ANDA077824	Amneal Pharmaceuticals of New York LLC	RANITIDINE HYDROCHLORIDE	150 mg/1	180 TABLET in 1 BOTTLE (53746-253-18)
53746-253-60	53746-253	HUMAN PRESCRIPTION DRUG	Ranitidine	Ranitidine	TABLET	ORAL	20091216	N/A	ANDA	ANDA077824	Amneal Pharmaceuticals of New York LLC	RANITIDINE HYDROCHLORIDE	150 mg/1	60 TABLET in 1 BOTTLE (53746-253-60)
53746-254-01	53746-254	HUMAN PRESCRIPTION DRUG	Ranitidine	Ranitidine	TABLET	ORAL	20091216	N/A	ANDA	ANDA077824	Amneal Pharmaceuticals of New York LLC	RANITIDINE HYDROCHLORIDE	300 mg/1	100 TABLET in 1 BOTTLE (53746-254-01)
53746-254-02	53746-254	HUMAN PRESCRIPTION DRUG	Ranitidine	Ranitidine	TABLET	ORAL	20091216	N/A	ANDA	ANDA077824	Amneal Pharmaceuticals of New York LLC	RANITIDINE HYDROCHLORIDE	300 mg/1	250 TABLET in 1 BOTTLE (53746-254-02)
53746-254-30	53746-254	HUMAN PRESCRIPTION DRUG	Ranitidine	Ranitidine	TABLET	ORAL	20091216	N/A	ANDA	ANDA077824	Amneal Pharmaceuticals of New York LLC	RANITIDINE HYDROCHLORIDE	300 mg/1	30 TABLET in 1 BOTTLE (53746-254-30)