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
70069-854-80	70069-854	HUMAN PRESCRIPTION DRUG	Sacubitril and Valsartan	Sacubitril and Valsartan	TABLET, FILM COATED	ORAL	20260221	N/A	ANDA	ANDA219983	Somerset Therapeutics, LLC	SACUBITRIL; VALSARTAN	49 mg/1; 51 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70069-854-80)
70069-854-60	70069-854	HUMAN PRESCRIPTION DRUG	Sacubitril and Valsartan	Sacubitril and Valsartan	TABLET, FILM COATED	ORAL	20260221	N/A	ANDA	ANDA219983	Somerset Therapeutics, LLC	SACUBITRIL; VALSARTAN	49 mg/1; 51 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70069-854-60)
70069-855-80	70069-855	HUMAN PRESCRIPTION DRUG	Sacubitril and Valsartan	Sacubitril and Valsartan	TABLET, FILM COATED	ORAL	20260221	N/A	ANDA	ANDA219983	Somerset Therapeutics, LLC	SACUBITRIL; VALSARTAN	97 mg/1; 103 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70069-855-80)
70069-855-60	70069-855	HUMAN PRESCRIPTION DRUG	Sacubitril and Valsartan	Sacubitril and Valsartan	TABLET, FILM COATED	ORAL	20260221	N/A	ANDA	ANDA219983	Somerset Therapeutics, LLC	SACUBITRIL; VALSARTAN	97 mg/1; 103 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70069-855-60)
70069-853-60	70069-853	HUMAN PRESCRIPTION DRUG	Sacubitril and Valsartan	Sacubitril and Valsartan	TABLET, FILM COATED	ORAL	20260221	N/A	ANDA	ANDA219983	Somerset Therapeutics, LLC	SACUBITRIL; VALSARTAN	24 mg/1; 26 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (70069-853-60)
70069-853-80	70069-853	HUMAN PRESCRIPTION DRUG	Sacubitril and Valsartan	Sacubitril and Valsartan	TABLET, FILM COATED	ORAL	20260221	N/A	ANDA	ANDA219983	Somerset Therapeutics, LLC	SACUBITRIL; VALSARTAN	24 mg/1; 26 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (70069-853-80)