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
0904-6583-04	0904-6583	HUMAN PRESCRIPTION DRUG	LAMIVUDINE	lamivudine	TABLET, FILM COATED	ORAL	20111202	N/A	ANDA	ANDA091606	Major Pharmaceuticals	LAMIVUDINE	150 mg/1	30 BLISTER PACK in 1 CARTON (0904-6583-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
60687-720-21	60687-720	HUMAN PRESCRIPTION DRUG	Lamivudine	Lamivudine	TABLET, FILM COATED	ORAL	20230119	N/A	ANDA	ANDA091606	American Health Packaging	LAMIVUDINE	150 mg/1	30 BLISTER PACK in 1 CARTON (60687-720-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-720-11)
60429-354-30	60429-354	HUMAN PRESCRIPTION DRUG	LAMIVUDINE	lamivudine	TABLET, FILM COATED	ORAL	20111202	N/A	ANDA	ANDA091606	Golden State Medical Supply, Inc.	LAMIVUDINE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60429-354-30)
60505-3252-3	60505-3252	HUMAN PRESCRIPTION DRUG	LAMIVUDINE	lamivudine	TABLET, FILM COATED	ORAL	20111202	N/A	ANDA	ANDA091606	Apotex Corp.	LAMIVUDINE	300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-3252-3)
60505-3252-8	60505-3252	HUMAN PRESCRIPTION DRUG	LAMIVUDINE	lamivudine	TABLET, FILM COATED	ORAL	20111202	N/A	ANDA	ANDA091606	Apotex Corp.	LAMIVUDINE	300 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-3252-8)
60429-353-60	60429-353	HUMAN PRESCRIPTION DRUG	LAMIVUDINE	lamivudine	TABLET, FILM COATED	ORAL	20111202	N/A	ANDA	ANDA091606	Golden State Medical Supply, Inc.	LAMIVUDINE	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (60429-353-60)
60505-3251-6	60505-3251	HUMAN PRESCRIPTION DRUG	LAMIVUDINE	lamivudine	TABLET, FILM COATED	ORAL	20111202	N/A	ANDA	ANDA091606	Apotex Corp.	LAMIVUDINE	150 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (60505-3251-6)
60505-3251-8	60505-3251	HUMAN PRESCRIPTION DRUG	LAMIVUDINE	lamivudine	TABLET, FILM COATED	ORAL	20111202	N/A	ANDA	ANDA091606	Apotex Corp.	LAMIVUDINE	150 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-3251-8)