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
70710-1367-9	70710-1367	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20210324	N/A	ANDA	ANDA212689	Zydus Pharmaceuticals USA Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70710-1367-9)
70710-1364-9	70710-1364	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA212689	Zydus Pharmaceuticals USA Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	100 mg/1; 150 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70710-1364-9)
70710-1365-3	70710-1365	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA212689	Zydus Pharmaceuticals USA Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	133 mg/1; 200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70710-1365-3)
70710-1364-3	70710-1364	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA212689	Zydus Pharmaceuticals USA Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	100 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70710-1364-3)