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
70771-1622-9	70771-1622	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA212689	Zydus Lifesciences Limited	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	167 mg/1; 250 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1622-9)
70771-1709-3	70771-1709	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20210324	N/A	ANDA	ANDA212689	Zydus Lifesciences Limited	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1709-3)
70771-1709-4	70771-1709	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20210324	N/A	ANDA	ANDA212689	Zydus Lifesciences Limited	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	10 BLISTER PACK in 1 CARTON (70771-1709-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1709-2)
70771-1709-9	70771-1709	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20210324	N/A	ANDA	ANDA212689	Zydus Lifesciences Limited	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1709-9)
60687-719-25	60687-719	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20231023	20260331	ANDA	ANDA212689	American Health Packaging	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	30 BLISTER PACK in 1 CARTON (60687-719-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-719-95)