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
59762-5014-1	59762-5014	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	spironolactone and hydrochlorothiazide	TABLET, FILM COATED	ORAL	19780101	N/A	NDA AUTHORIZED GENERIC	NDA012616	Greenstone LLC	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59762-5014-1)
0025-1021-31	0025-1021	HUMAN PRESCRIPTION DRUG	ALDACTAZIDE	spironolactone and hydrochlorothiazide	TABLET, FILM COATED	ORAL	19780101	20250131	NDA	NDA012616	Pfizer Laboratories Div Pfizer Inc	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	50 mg/1; 50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0025-1021-31)
66993-188-02	66993-188	HUMAN PRESCRIPTION DRUG	Spironolactone and Hydrochlorothiazide	spironolactone and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20211129	N/A	NDA AUTHORIZED GENERIC	NDA012616	Prasco Laboratories	HYDROCHLOROTHIAZIDE; SPIRONOLACTONE	25 mg/1; 25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (66993-188-02)