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
31722-752-60	31722-752	HUMAN PRESCRIPTION DRUG	Lamivudine	Lamivudine	TABLET, FILM COATED	ORAL	20140102	N/A	ANDA	ANDA203260	Camber Pharmaceuticals, Inc.	LAMIVUDINE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (31722-752-60)
31722-752-32	31722-752	HUMAN PRESCRIPTION DRUG	Lamivudine	Lamivudine	TABLET, FILM COATED	ORAL	20140102	N/A	ANDA	ANDA203260	Camber Pharmaceuticals, Inc.	LAMIVUDINE	100 mg/1	100 TABLET, FILM COATED in 1 CARTON (31722-752-32)
31722-752-31	31722-752	HUMAN PRESCRIPTION DRUG	Lamivudine	Lamivudine	TABLET, FILM COATED	ORAL	20140102	N/A	ANDA	ANDA203260	Camber Pharmaceuticals, Inc.	LAMIVUDINE	100 mg/1	10 TABLET, FILM COATED in 1 BLISTER PACK (31722-752-31)
31722-752-06	31722-752	HUMAN PRESCRIPTION DRUG	Lamivudine	Lamivudine	TABLET, FILM COATED	ORAL	20140102	N/A	ANDA	ANDA203260	Camber Pharmaceuticals, Inc.	LAMIVUDINE	100 mg/1	600 TABLET, FILM COATED in 1 BOTTLE (31722-752-06)