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
31722-560-30	31722-560	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA201806	Camber Pharmaceuticals, Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-560-30)
50090-7719-1	50090-7719	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20251016	N/A	ANDA	ANDA201806	A-S Medication Solutions	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-7719-1)
67296-2198-5	67296-2198	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA201806	Redpharm Drug	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	5 TABLET, FILM COATED in 1 BOTTLE (67296-2198-5)
67296-2198-3	67296-2198	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20211007	N/A	ANDA	ANDA201806	Redpharm Drug	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (67296-2198-3)
68071-3831-3	68071-3831	HUMAN PRESCRIPTION DRUG	Emtricitabine and tenofovir disoproxil fumarate	Emtricitabine and tenofovir disoproxil fumarate	TABLET, FILM COATED	ORAL	20250418	N/A	ANDA	ANDA201806	NuCare Pharmaceuticals, Inc.	EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE	200 mg/1; 300 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (68071-3831-3)