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
71335-0141-1	71335-0141	HUMAN PRESCRIPTION DRUG	Lamivudine and Zidovudine	Lamivudine and Zidovudine	TABLET	ORAL	20161210	N/A	ANDA	ANDA079128	Bryant Ranch Prepack	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	6 TABLET in 1 BOTTLE (71335-0141-1)
71335-0141-2	71335-0141	HUMAN PRESCRIPTION DRUG	Lamivudine and Zidovudine	Lamivudine and Zidovudine	TABLET	ORAL	20161210	N/A	ANDA	ANDA079128	Bryant Ranch Prepack	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	60 TABLET in 1 BOTTLE (71335-0141-2)
71335-0141-3	71335-0141	HUMAN PRESCRIPTION DRUG	Lamivudine and Zidovudine	Lamivudine and Zidovudine	TABLET	ORAL	20161210	N/A	ANDA	ANDA079128	Bryant Ranch Prepack	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	4 TABLET in 1 BOTTLE (71335-0141-3)
64380-707-03	64380-707	HUMAN PRESCRIPTION DRUG	Lamivudine and Zidovudine	Lamivudine and Zidovudine	TABLET	ORAL	20161210	N/A	ANDA	ANDA079128	Strides Pharma Science Limited	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	60 TABLET in 1 BOTTLE (64380-707-03)