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
69097-209-02	69097-209	HUMAN PRESCRIPTION DRUG	EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE	EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE	TABLET, FILM COATED	ORAL	20210330	N/A	ANDA	ANDA090958	Cipla USA Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-209-02)
69097-741-02	69097-741	HUMAN PRESCRIPTION DRUG	EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE	EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE	TABLET, FILM COATED	ORAL	20211101	N/A	ANDA	ANDA090958	Cipla USA Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-741-02)
76282-677-30	76282-677	HUMAN PRESCRIPTION DRUG	EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE	EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE	TABLET, FILM COATED	ORAL	20210406	N/A	ANDA	ANDA090958	Exelan Pharmaceuticals, Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76282-677-30)