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
63629-1068-1	63629-1068	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	19870702	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (63629-1068-1)
63629-1071-2	63629-1071	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	20200924	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (63629-1071-2)
53489-144-01	53489-144	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	19870702	N/A	ANDA	ANDA089534	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (53489-144-01)
53489-144-05	53489-144	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	19870702	N/A	ANDA	ANDA089534	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (53489-144-05)
53489-144-10	53489-144	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	19870702	N/A	ANDA	ANDA089534	Sun Pharmaceutical Industries, Inc.	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (53489-144-10)
71335-2202-1	71335-2202	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	20230804	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (71335-2202-1)
63629-1071-1	63629-1071	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	20200915	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (63629-1071-1)
63629-1069-1	63629-1069	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	19870702	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (63629-1069-1)
63629-1071-3	63629-1071	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	20200921	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (63629-1071-3)
72162-1625-1	72162-1625	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	20230927	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (72162-1625-1)
72162-1625-3	72162-1625	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	20230927	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72162-1625-3)
72162-1625-5	72162-1625	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	20230927	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (72162-1625-5)
72162-1625-6	72162-1625	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	Spironolactone and Hydrochlorothiazide	TABLET	ORAL	20230927	N/A	ANDA	ANDA089534	Bryant Ranch Prepack	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (72162-1625-6)