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
70771-1053-3	70771-1053	HUMAN PRESCRIPTION DRUG	Abacavir and lamivudine	Abacavir and lamivudine	TABLET, FILM COATED	ORAL	20190314	N/A	ANDA	ANDA208990	Zydus Lifesciences Limited	ABACAVIR SULFATE; LAMIVUDINE	600 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1053-3)
70771-1053-9	70771-1053	HUMAN PRESCRIPTION DRUG	Abacavir and lamivudine	Abacavir and lamivudine	TABLET, FILM COATED	ORAL	20190314	N/A	ANDA	ANDA208990	Zydus Lifesciences Limited	ABACAVIR SULFATE; LAMIVUDINE	600 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1053-9)
70710-1049-3	70710-1049	HUMAN PRESCRIPTION DRUG	Abacavir and lamivudine	Abacavir and lamivudine	TABLET, FILM COATED	ORAL	20190314	N/A	ANDA	ANDA208990	Zydus Pharmaceuticals USA Inc.	ABACAVIR SULFATE; LAMIVUDINE	600 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70710-1049-3)
70710-1049-9	70710-1049	HUMAN PRESCRIPTION DRUG	Abacavir and lamivudine	Abacavir and lamivudine	TABLET, FILM COATED	ORAL	20190314	N/A	ANDA	ANDA208990	Zydus Pharmaceuticals USA Inc.	ABACAVIR SULFATE; LAMIVUDINE	600 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70710-1049-9)