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
43063-900-06	43063-900	HUMAN PRESCRIPTION DRUG	LAMIVUDINE and ZIDOVUDINE	LAMIVUDINE and ZIDOVUDINE	TABLET, FILM COATED	ORAL	20181011	N/A	ANDA	ANDA079124	PD-Rx Pharmaceuticals, Inc.	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-900-06)
31722-506-05	31722-506	HUMAN PRESCRIPTION DRUG	LAMIVUDINE and ZIDOVUDINE	LAMIVUDINE and ZIDOVUDINE	TABLET, FILM COATED	ORAL	20150918	N/A	ANDA	ANDA079124	Camber Pharmaceuticals, Inc.	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-506-05)
31722-506-60	31722-506	HUMAN PRESCRIPTION DRUG	LAMIVUDINE and ZIDOVUDINE	LAMIVUDINE and ZIDOVUDINE	TABLET, FILM COATED	ORAL	20150918	N/A	ANDA	ANDA079124	Camber Pharmaceuticals, Inc.	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (31722-506-60)
71335-0639-1	71335-0639	HUMAN PRESCRIPTION DRUG	LAMIVUDINE and ZIDOVUDINE	LAMIVUDINE and ZIDOVUDINE	TABLET, FILM COATED	ORAL	20210402	N/A	ANDA	ANDA079124	Bryant Ranch Prepack	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71335-0639-1)
71335-0639-2	71335-0639	HUMAN PRESCRIPTION DRUG	LAMIVUDINE and ZIDOVUDINE	LAMIVUDINE and ZIDOVUDINE	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA079124	Bryant Ranch Prepack	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0639-2)
71335-0639-3	71335-0639	HUMAN PRESCRIPTION DRUG	LAMIVUDINE and ZIDOVUDINE	LAMIVUDINE and ZIDOVUDINE	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA079124	Bryant Ranch Prepack	LAMIVUDINE; ZIDOVUDINE	150 mg/1; 300 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (71335-0639-3)