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
76282-115-60	76282-115	HUMAN PRESCRIPTION DRUG	Lamivudine and Zidovudine	Lamivudine and Zidovudine	TABLET, FILM COATED	ORAL	20150429	N/A	ANDA	ANDA203259	Exelan Pharmaceuticals Inc.	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76282-115-60)
76282-115-05	76282-115	HUMAN PRESCRIPTION DRUG	Lamivudine and Zidovudine	Lamivudine and Zidovudine	TABLET, FILM COATED	ORAL	20150429	N/A	ANDA	ANDA203259	Exelan Pharmaceuticals Inc.	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76282-115-05)
72865-144-60	72865-144	HUMAN PRESCRIPTION DRUG	LAMIVUDINE AND ZIDOVUDINE	lamivudine and zidovudine	TABLET, FILM COATED	ORAL	20200417	N/A	ANDA	ANDA203259	XLCare Pharmaceuticals, Inc	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72865-144-60)
31722-739-05	31722-739	HUMAN PRESCRIPTION DRUG	Lamivudine and Zidovudine	Lamivudine and Zidovudine	TABLET, FILM COATED	ORAL	20140206	N/A	ANDA	ANDA203259	Camber Pharmaceuticals, Inc.	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-739-05)
31722-739-31	31722-739	HUMAN PRESCRIPTION DRUG	Lamivudine and Zidovudine	Lamivudine and Zidovudine	TABLET, FILM COATED	ORAL	20140206	N/A	ANDA	ANDA203259	Camber Pharmaceuticals, Inc.	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	100 TABLET, FILM COATED in 1 BLISTER PACK (31722-739-31)
31722-739-60	31722-739	HUMAN PRESCRIPTION DRUG	Lamivudine and Zidovudine	Lamivudine and Zidovudine	TABLET, FILM COATED	ORAL	20140206	N/A	ANDA	ANDA203259	Camber Pharmaceuticals, Inc.	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (31722-739-60)