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
67296-1433-3	67296-1433	HUMAN PRESCRIPTION DRUG	Emtricitabine and Tenofovir Disoproxil Fumarate	Emtricitabine and Tenofovir Disoproxil Fumarate	TABLET, FILM COATED	ORAL	20210401	N/A	ANDA	ANDA090894	RedPharm Drug, Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (67296-1433-3)
72189-156-02	72189-156	HUMAN PRESCRIPTION DRUG	EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE	EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE	TABLET, FILM COATED	ORAL	20201119	N/A	ANDA	ANDA090894	Direct Rx	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (72189-156-02)
0093-7704-56	0093-7704	HUMAN PRESCRIPTION DRUG	Emtricitabine and Tenofovir Disoproxil Fumarate	Emtricitabine and Tenofovir Disoproxil Fumarate	TABLET, FILM COATED	ORAL	20210120	N/A	ANDA	ANDA090894	Teva Pharmaceuticals USA, Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-7704-56)