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
59651-165-30	59651-165	HUMAN PRESCRIPTION DRUG	Emtricitabine and Tenofovir Disoproxil Fumarate	Emtricitabine and Tenofovir Disoproxil Fumarate	TABLET, FILM COATED	ORAL	20230309	N/A	ANDA	ANDA211640	Aurobindo Pharma Limited	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	100 mg/1; 150 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-165-30)
59651-166-30	59651-166	HUMAN PRESCRIPTION DRUG	Emtricitabine and Tenofovir Disoproxil Fumarate	Emtricitabine and Tenofovir Disoproxil Fumarate	TABLET, FILM COATED	ORAL	20230309	N/A	ANDA	ANDA211640	Aurobindo Pharma Limited	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	133 mg/1; 200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-166-30)
59651-167-30	59651-167	HUMAN PRESCRIPTION DRUG	Emtricitabine and Tenofovir Disoproxil Fumarate	Emtricitabine and Tenofovir Disoproxil Fumarate	TABLET, FILM COATED	ORAL	20230309	N/A	ANDA	ANDA211640	Aurobindo Pharma Limited	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	167 mg/1; 250 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-167-30)